MAP3K14 (mitogen-activated protein kinase kinase kinase 14) - Rat Genome Database

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Gene: MAP3K14 (mitogen-activated protein kinase kinase kinase 14) Homo sapiens
Analyze
Symbol: MAP3K14
Name: mitogen-activated protein kinase kinase kinase 14
RGD ID: 1321416
HGNC Page HGNC:6853
Description: Enables protein serine/threonine kinase activity. Involved in cellular response to mechanical stimulus and non-canonical NF-kappaB signal transduction. Located in cytosol; fibrillar center; and nucleoplasm. Implicated in primary immunodeficiency disease.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FTDCR1B; HS; HSNIK; IMD112; NF-kappa-beta-inducing kinase; NIK; serine/threonine protein-kinase; serine/threonine-protein kinase NIK
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381745,263,119 - 45,317,020 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1745,263,119 - 45,317,029 (-)EnsemblGRCh38hg38GRCh38
GRCh371743,340,486 - 43,394,386 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361740,696,271 - 40,750,197 (-)NCBINCBI36Build 36hg18NCBI36
Build 341740,696,277 - 40,724,123NCBI
Celera1740,049,855 - 40,103,781 (-)NCBICelera
Cytogenetic Map17q21.31NCBI
HuRef1739,101,255 - 39,155,179 (-)NCBIHuRef
CHM1_11743,575,752 - 43,629,721 (-)NCBICHM1_1
T2T-CHM13v2.01746,116,902 - 46,170,784 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-epigallocatechin 3-gallate  (EXP)
1'-acetoxychavicol acetate  (EXP)
1,2-dichloroethane  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-Hydroxy-6-(8,11,14-pentadecatrienyl)benzoic acid  (EXP)
2-hydroxyethyl methacrylate  (EXP)
2-palmitoylglycerol  (EXP)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3-phenylprop-2-enal  (ISO)
4-nitrophenol  (ISO)
acrylamide  (EXP)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP)
benzo[e]pyrene  (EXP)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
butanal  (EXP)
cadmium atom  (EXP)
calcitriol  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
ciguatoxin CTX1B  (ISO)
cisplatin  (EXP)
copper atom  (EXP)
copper(0)  (EXP)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
cylindrospermopsin  (EXP)
dexamethasone  (EXP)
diallyl trisulfide  (EXP)
dicrotophos  (EXP)
dieldrin  (EXP)
dimethylarsinic acid  (ISO)
disodium selenite  (EXP)
dorsomorphin  (EXP)
Fusarenone X  (ISO)
genistein  (EXP)
gentamycin  (ISO)
ibrutinib  (EXP)
indometacin  (EXP)
iron atom  (ISO)
iron(0)  (ISO)
iron(2+) sulfate (anhydrous)  (ISO)
leflunomide  (EXP)
Licochalcone B  (EXP)
lipopolysaccharide  (EXP,ISO)
manganese atom  (ISO)
manganese(0)  (ISO)
mangiferin  (EXP)
mercury dibromide  (EXP)
metacetamol  (ISO)
methapyrilene  (EXP)
methotrexate  (EXP)
methylmercury chloride  (EXP)
N-methyl-4-phenylpyridinium  (EXP)
nickel atom  (EXP)
nickel sulfate  (EXP)
o-anisidine  (EXP)
obeticholic acid  (EXP)
ochratoxin A  (EXP)
p-chloromercuribenzoic acid  (EXP)
p-menthan-3-ol  (EXP)
paracetamol  (EXP,ISO)
pentachlorophenol  (ISO)
perfluorohexanesulfonic acid  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (EXP)
perfluorooctanoic acid  (EXP)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
phorbol 13-acetate 12-myristate  (EXP)
pirinixic acid  (EXP,ISO)
potassium chromate  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP,ISO)
silver atom  (EXP)
silver(0)  (EXP)
simvastatin  (EXP)
SM-164  (EXP)
sodium arsenite  (EXP)
sulfates  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
tetraphene  (ISO)
thioacetamide  (ISO)
trichloroethene  (ISO)
Tylophorine  (EXP)
urethane  (EXP)
valproic acid  (EXP)
vanadium atom  (EXP)
vanadium(0)  (EXP)
zerumbone  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Shared principles in NF-kappaB signaling. Hayden MS and Ghosh S, Cell. 2008 Feb 8;132(3):344-62.
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9020361   PMID:9244310   PMID:9275204   PMID:9346485   PMID:9520446   PMID:9689078   PMID:9742107   PMID:9751059   PMID:9799091   PMID:9819420   PMID:9927690   PMID:10022904  
PMID:10072079   PMID:10094049   PMID:10195894   PMID:10521444   PMID:10733566   PMID:10779355   PMID:10807933   PMID:10887201   PMID:10921914   PMID:11002417   PMID:11035039   PMID:11116146  
PMID:11239468   PMID:11278268   PMID:11369779   PMID:11511100   PMID:11585904   PMID:11801607   PMID:12049732   PMID:12185077   PMID:12393548   PMID:12477932   PMID:12853971   PMID:12874243  
PMID:12884866   PMID:14743126   PMID:14743216   PMID:15001576   PMID:15084608   PMID:15208311   PMID:15252129   PMID:15489334   PMID:16009713   PMID:16286467   PMID:16344560   PMID:16498412  
PMID:17158868   PMID:17237370   PMID:17543278   PMID:17563756   PMID:17620599   PMID:17729113   PMID:18022362   PMID:18029348   PMID:18056702   PMID:18434448   PMID:18439422   PMID:18752500  
PMID:18976975   PMID:19262425   PMID:19453261   PMID:19593445   PMID:19641626   PMID:19641890   PMID:19646419   PMID:19897484   PMID:19909783   PMID:20125184   PMID:20184394   PMID:20338663  
PMID:20348096   PMID:20385093   PMID:20466000   PMID:20501937   PMID:20682767   PMID:20735436   PMID:20823135   PMID:20937806   PMID:21048031   PMID:21257964   PMID:21273489   PMID:21478870  
PMID:21833088   PMID:21846802   PMID:21869881   PMID:21873635   PMID:21887257   PMID:21900206   PMID:21963849   PMID:22105365   PMID:22469134   PMID:22474019   PMID:22685329   PMID:22718757  
PMID:22939624   PMID:22968463   PMID:23301098   PMID:23536439   PMID:23543740   PMID:24362935   PMID:24533079   PMID:25036637   PMID:25043127   PMID:25079338   PMID:25184681   PMID:25187543  
PMID:25241761   PMID:25246529   PMID:25406581   PMID:25416956   PMID:25622756   PMID:25766331   PMID:26178280   PMID:26195760   PMID:26269411   PMID:26498133   PMID:26602079   PMID:26823811  
PMID:27197231   PMID:27416764   PMID:27499151   PMID:27555280   PMID:27678221   PMID:27876836   PMID:27889261   PMID:27905294   PMID:28005357   PMID:28049766   PMID:28379340   PMID:28448599  
PMID:28514442   PMID:28947934   PMID:29061763   PMID:29116141   PMID:29230214   PMID:29283461   PMID:29284006   PMID:29320732   PMID:29326084   PMID:29329668   PMID:29330524   PMID:29407886  
PMID:29483833   PMID:29503445   PMID:29533931   PMID:29555915   PMID:29654269   PMID:29728424   PMID:30018345   PMID:30335132   PMID:30745168   PMID:30833792   PMID:30837284   PMID:30894749  
PMID:31246323   PMID:31391242   PMID:31768922   PMID:31980649   PMID:32028675   PMID:32296183   PMID:32469170   PMID:32707033   PMID:32759710   PMID:32814053   PMID:33198776   PMID:33723235  
PMID:33961781   PMID:35165513   PMID:36190381   PMID:36356831   PMID:36931259   PMID:37165186   PMID:37461228   PMID:37567906  


Genomics

Comparative Map Data
MAP3K14
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381745,263,119 - 45,317,020 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1745,263,119 - 45,317,029 (-)EnsemblGRCh38hg38GRCh38
GRCh371743,340,486 - 43,394,386 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361740,696,271 - 40,750,197 (-)NCBINCBI36Build 36hg18NCBI36
Build 341740,696,277 - 40,724,123NCBI
Celera1740,049,855 - 40,103,781 (-)NCBICelera
Cytogenetic Map17q21.31NCBI
HuRef1739,101,255 - 39,155,179 (-)NCBIHuRef
CHM1_11743,575,752 - 43,629,721 (-)NCBICHM1_1
T2T-CHM13v2.01746,116,902 - 46,170,784 (-)NCBIT2T-CHM13v2.0
Map3k14
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911103,110,590 - 103,158,227 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl11103,110,588 - 103,158,298 (-)EnsemblGRCm39 Ensembl
GRCm3811103,219,764 - 103,267,401 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11103,219,762 - 103,267,472 (-)EnsemblGRCm38mm10GRCm38
MGSCv3711103,081,078 - 103,128,715 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3611103,035,854 - 103,083,491 (-)NCBIMGSCv36mm8
Celera11114,933,508 - 114,981,179 (-)NCBICelera
Cytogenetic Map11E1NCBI
cM Map1166.8NCBI
Map3k14
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81088,665,417 - 88,715,669 (-)NCBIGRCr8
mRatBN7.21088,165,349 - 88,215,558 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1088,165,351 - 88,215,523 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1093,201,107 - 93,251,268 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01092,668,001 - 92,718,220 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01088,061,351 - 88,111,570 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01091,303,428 - 91,353,601 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1091,303,428 - 91,353,601 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01091,074,396 - 91,121,436 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41092,406,098 - 92,456,276 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11092,421,198 - 92,444,501 (-)NCBI
Celera1086,866,471 - 86,916,375 (-)NCBICelera
Cytogenetic Map10q32.1NCBI
Map3k14
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545117,908,827 - 17,926,151 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545117,907,800 - 17,954,821 (-)NCBIChiLan1.0ChiLan1.0
MAP3K14
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21919,521,228 - 19,575,128 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11721,489,935 - 21,543,815 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01712,011,037 - 12,064,978 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11712,183,243 - 12,237,131 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1712,183,243 - 12,237,131 (+)Ensemblpanpan1.1panPan2
MAP3K14
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1918,255,416 - 18,302,405 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl918,280,198 - 18,302,401 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha917,640,218 - 17,687,188 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0918,928,453 - 18,975,466 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl918,928,497 - 18,975,502 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1917,806,803 - 17,853,778 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0917,985,479 - 18,032,427 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0918,141,265 - 18,188,242 (+)NCBIUU_Cfam_GSD_1.0
Map3k14
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560217,602,812 - 17,645,706 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365411,548,875 - 1,591,833 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365411,548,892 - 1,591,770 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MAP3K14
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1218,142,952 - 18,182,928 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11218,142,899 - 18,182,931 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21218,391,601 - 18,431,641 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MAP3K14
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11661,100,298 - 61,153,984 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1661,100,352 - 61,155,052 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607731,837,235 - 31,890,835 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Map3k14
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624795167,990 - 203,784 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624795167,959 - 207,421 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MAP3K14
431 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_003954.5(MAP3K14):c.764C>T (p.Thr255Met) single nucleotide variant NIK deficiency [RCV001422903] Chr17:45286819 [GRCh38]
Chr17:43364186 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.132C>T (p.Ala44=) single nucleotide variant NIK deficiency [RCV000541968]|not provided [RCV001811074] Chr17:45290614 [GRCh38]
Chr17:43367980 [GRCh37]
Chr17:17q21.31		 benign
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
NM_003954.5(MAP3K14):c.2290A>G (p.Thr764Ala) single nucleotide variant NIK deficiency [RCV000554433]|not provided [RCV001811075] Chr17:45267442 [GRCh38]
Chr17:43344809 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.4(MAP3K14):c.-20-4133T>C single nucleotide variant Lung cancer [RCV000100477] Chr17:45294898 [GRCh38]
Chr17:43372264 [GRCh37]
Chr17:17q21.31		 uncertain significance
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3 copy number gain See cases [RCV000052479] Chr17:39199873..45629579 [GRCh38]
Chr17:37356126..43706945 [GRCh37]
Chr17:34609652..41062728 [NCBI36]
Chr17:17q12-21.31		 pathogenic
GRCh38/hg38 17q21.31-21.33(chr17:44955325-49381173)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|See cases [RCV000052480] Chr17:44955325..49381173 [GRCh38]
Chr17:43032693..47458535 [GRCh37]
Chr17:40388219..44813534 [NCBI36]
Chr17:17q21.31-21.33		 pathogenic
GRCh38/hg38 17q21.31(chr17:44928498-45299730)x1 copy number loss See cases [RCV000053430] Chr17:44928498..45299730 [GRCh38]
Chr17:43005866..43377096 [GRCh37]
Chr17:40361392..40732879 [NCBI36]
Chr17:17q21.31		 pathogenic
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_003954.5(MAP3K14):c.1720G>A (p.Asp574Asn) single nucleotide variant NIK deficiency [RCV000698152] Chr17:45271159 [GRCh38]
Chr17:43348526 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2820T>C (p.His940=) single nucleotide variant NIK deficiency [RCV000529903] Chr17:45264660 [GRCh38]
Chr17:43342027 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1290+5G>A single nucleotide variant NIK deficiency [RCV000655439] Chr17:45284807 [GRCh38]
Chr17:43362174 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.296G>A (p.Arg99His) single nucleotide variant NIK deficiency [RCV000655440] Chr17:45289266 [GRCh38]
Chr17:43366632 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.820C>T (p.Pro274Ser) single nucleotide variant NIK deficiency [RCV000655441] Chr17:45286763 [GRCh38]
Chr17:43364130 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.823T>C (p.Trp275Arg) single nucleotide variant NIK deficiency [RCV000655442] Chr17:45286760 [GRCh38]
Chr17:43364127 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.916T>C (p.Cys306Arg) single nucleotide variant NIK deficiency [RCV000655443] Chr17:45286667 [GRCh38]
Chr17:43364034 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2312A>C (p.Gln771Pro) single nucleotide variant NIK deficiency [RCV000655444] Chr17:45267420 [GRCh38]
Chr17:43344787 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1546G>A (p.Val516Ile) single nucleotide variant NIK deficiency [RCV000655445]|not provided [RCV001729677] Chr17:45274129 [GRCh38]
Chr17:43351496 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.880A>C (p.Lys294Gln) single nucleotide variant NIK deficiency [RCV000655446]|not provided [RCV003411557] Chr17:45286703 [GRCh38]
Chr17:43364070 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.521G>A (p.Cys174Tyr) single nucleotide variant MAP3K14-related condition [RCV003938004]|NIK deficiency [RCV000655447] Chr17:45287170 [GRCh38]
Chr17:43364536 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.1587C>T (p.His529=) single nucleotide variant NIK deficiency [RCV000655448] Chr17:45273573 [GRCh38]
Chr17:43350940 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.419G>A (p.Ser140Asn) single nucleotide variant NIK deficiency [RCV000655449]|not provided [RCV001811432] Chr17:45287272 [GRCh38]
Chr17:43364638 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.326+10G>A single nucleotide variant NIK deficiency [RCV000655450]|not provided [RCV001729678] Chr17:45289226 [GRCh38]
Chr17:43366592 [GRCh37]
Chr17:17q21.31		 benign|likely benign
NM_003954.5(MAP3K14):c.774C>G (p.Phe258Leu) single nucleotide variant NIK deficiency [RCV000655451] Chr17:45286809 [GRCh38]
Chr17:43364176 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.555C>T (p.Leu185=) single nucleotide variant NIK deficiency [RCV000655452]|not provided [RCV003424261] Chr17:45287028 [GRCh38]
Chr17:43364394 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2020C>T (p.His674Tyr) single nucleotide variant NIK deficiency [RCV000655453] Chr17:45267712 [GRCh38]
Chr17:43345079 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.2292C>T (p.Thr764=) single nucleotide variant NIK deficiency [RCV000655454] Chr17:45267440 [GRCh38]
Chr17:43344807 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1009C>T (p.Leu337=) single nucleotide variant NIK deficiency [RCV000655455]|not provided [RCV003411558] Chr17:45286574 [GRCh38]
Chr17:43363941 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2434-10G>A single nucleotide variant NIK deficiency [RCV000655456]|not provided [RCV001702830] Chr17:45266691 [GRCh38]
Chr17:43344058 [GRCh37]
Chr17:17q21.31		 benign|likely benign
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q21.31(chr17:42649083-43659985)x3 copy number gain See cases [RCV000512371] Chr17:42649083..43659985 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1651C>G (p.Leu551Val) single nucleotide variant NIK deficiency [RCV000700178] Chr17:45273509 [GRCh38]
Chr17:43350876 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.643G>A (p.Glu215Lys) single nucleotide variant NIK deficiency [RCV000687892] Chr17:45286940 [GRCh38]
Chr17:43364306 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.115G>A (p.Val39Ile) single nucleotide variant NIK deficiency [RCV000689609] Chr17:45290631 [GRCh38]
Chr17:43367997 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2779G>A (p.Ala927Thr) single nucleotide variant NIK deficiency [RCV000697363] Chr17:45264701 [GRCh38]
Chr17:43342068 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2433+3G>A single nucleotide variant NIK deficiency [RCV000696179] Chr17:45267089 [GRCh38]
Chr17:43344456 [GRCh37]
Chr17:17q21.31		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_003954.5(MAP3K14):c.2367G>A (p.Glu789=) single nucleotide variant NIK deficiency [RCV002066489] Chr17:45267158 [GRCh38]
Chr17:43344525 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2326+4C>T single nucleotide variant NIK deficiency [RCV001065890] Chr17:45267402 [GRCh38]
Chr17:43344769 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.114C>T (p.Ser38=) single nucleotide variant NIK deficiency [RCV000879838]|not provided [RCV001702062] Chr17:45290632 [GRCh38]
Chr17:43367998 [GRCh37]
Chr17:17q21.31		 benign|likely benign
NM_003954.5(MAP3K14):c.1455C>T (p.Gly485=) single nucleotide variant NIK deficiency [RCV000880842]|not specified [RCV001001959] Chr17:45274220 [GRCh38]
Chr17:43351587 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2679+7G>A single nucleotide variant NIK deficiency [RCV001501859] Chr17:45265156 [GRCh38]
Chr17:43342523 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2054C>T (p.Thr685Ile) single nucleotide variant NIK deficiency [RCV001040516] Chr17:45267678 [GRCh38]
Chr17:43345045 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2237C>T (p.Ser746Phe) single nucleotide variant NIK deficiency [RCV001069401] Chr17:45267495 [GRCh38]
Chr17:43344862 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1252G>A (p.Glu418Lys) single nucleotide variant NIK deficiency [RCV001062008] Chr17:45284850 [GRCh38]
Chr17:43362217 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2127_2128dup (p.Ala710fs) microsatellite NIK deficiency [RCV001039299] Chr17:45267603..45267604 [GRCh38]
Chr17:43344970..43344971 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.437G>A (p.Arg146Gln) single nucleotide variant NIK deficiency [RCV001039325] Chr17:45287254 [GRCh38]
Chr17:43364620 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1821+17A>C single nucleotide variant NIK deficiency [RCV001522658]|not provided [RCV001812324] Chr17:45271041 [GRCh38]
Chr17:43348408 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.488A>G (p.Lys163Arg) single nucleotide variant NIK deficiency [RCV001048394] Chr17:45287203 [GRCh38]
Chr17:43364569 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.64C>T (p.Leu22Phe) single nucleotide variant NIK deficiency [RCV001070202] Chr17:45290682 [GRCh38]
Chr17:43368048 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1830C>T (p.Ser610=) single nucleotide variant NIK deficiency [RCV003758925]|not provided [RCV000768262] Chr17:45270555 [GRCh38]
Chr17:43347922 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.715G>A (p.Val239Met) single nucleotide variant NIK deficiency [RCV001036220] Chr17:45286868 [GRCh38]
Chr17:43364235 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1657G>A (p.Gly553Arg) single nucleotide variant NIK deficiency [RCV000807656] Chr17:45273503 [GRCh38]
Chr17:43350870 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2418G>C (p.Ser806=) single nucleotide variant NIK deficiency [RCV001424850] Chr17:45267107 [GRCh38]
Chr17:43344474 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2628G>A (p.Arg876=) single nucleotide variant NIK deficiency [RCV001395803] Chr17:45265214 [GRCh38]
Chr17:43342581 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2418G>A (p.Ser806=) single nucleotide variant NIK deficiency [RCV000879171] Chr17:45267107 [GRCh38]
Chr17:43344474 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.918T>C (p.Cys306=) single nucleotide variant NIK deficiency [RCV001481003]|not provided [RCV003411903] Chr17:45286665 [GRCh38]
Chr17:43364032 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-7C>T single nucleotide variant NIK deficiency [RCV001473345] Chr17:45287052 [GRCh38]
Chr17:43364418 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.333C>T (p.Ser111=) single nucleotide variant NIK deficiency [RCV001437238] Chr17:45287358 [GRCh38]
Chr17:43364724 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.411G>C (p.Lys137Asn) single nucleotide variant NIK deficiency [RCV000799642] Chr17:45287280 [GRCh38]
Chr17:43364646 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2668A>G (p.Ile890Val) single nucleotide variant NIK deficiency [RCV000816323] Chr17:45265174 [GRCh38]
Chr17:43342541 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.656C>T (p.Pro219Leu) single nucleotide variant NIK deficiency [RCV000803284] Chr17:45286927 [GRCh38]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2096G>C (p.Gly699Ala) single nucleotide variant NIK deficiency [RCV000824177] Chr17:45267636 [GRCh38]
Chr17:43345003 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.727C>T (p.His243Tyr) single nucleotide variant NIK deficiency [RCV000798803] Chr17:45286856 [GRCh38]
Chr17:43364223 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.145C>G (p.Pro49Ala) single nucleotide variant NIK deficiency [RCV000808532] Chr17:45290601 [GRCh38]
Chr17:43367967 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1131C>T (p.Asn377=) single nucleotide variant NIK deficiency [RCV000976498] Chr17:45286452 [GRCh38]
Chr17:43363819 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.668G>A (p.Arg223Gln) single nucleotide variant NIK deficiency [RCV000809068] Chr17:45286915 [GRCh38]
Chr17:43364282 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2679+5G>A single nucleotide variant NIK deficiency [RCV000793261] Chr17:45265158 [GRCh38]
Chr17:43342525 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2543G>A (p.Arg848Gln) single nucleotide variant NIK deficiency [RCV000806361] Chr17:45266572 [GRCh38]
Chr17:43343939 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1420+4A>G single nucleotide variant NIK deficiency [RCV000797088] Chr17:45274460 [GRCh38]
Chr17:43351827 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1798T>C (p.Phe600Leu) single nucleotide variant NIK deficiency [RCV000817751] Chr17:45271081 [GRCh38]
Chr17:43348448 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2615A>G (p.His872Arg) single nucleotide variant NIK deficiency [RCV000818113] Chr17:45265227 [GRCh38]
Chr17:43342594 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1615G>C (p.Val539Leu) single nucleotide variant NIK deficiency [RCV001045219] Chr17:45273545 [GRCh38]
Chr17:43350912 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1091G>C (p.Gly364Ala) single nucleotide variant NIK deficiency [RCV000801938] Chr17:45286492 [GRCh38]
Chr17:43363859 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1794G>C (p.Gln598His) single nucleotide variant NIK deficiency [RCV000794406] Chr17:45271085 [GRCh38]
Chr17:43348452 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.307G>A (p.Ala103Thr) single nucleotide variant Inborn genetic diseases [RCV002535501]|NIK deficiency [RCV000819324] Chr17:45289255 [GRCh38]
Chr17:43366621 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2405G>C (p.Ser802Thr) single nucleotide variant NIK deficiency [RCV000822858] Chr17:45267120 [GRCh38]
Chr17:43344487 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.416G>A (p.Arg139His) single nucleotide variant NIK deficiency [RCV000895834] Chr17:45287275 [GRCh38]
Chr17:43364641 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.559G>A (p.Ala187Thr) single nucleotide variant NIK deficiency [RCV000792844] Chr17:45287024 [GRCh38]
Chr17:43364390 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.424G>T (p.Ala142Ser) single nucleotide variant NIK deficiency [RCV001219650] Chr17:45287267 [GRCh38]
Chr17:43364633 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.86C>T (p.Thr29Met) single nucleotide variant NIK deficiency [RCV001224589] Chr17:45290660 [GRCh38]
Chr17:43368026 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.742G>A (p.Gly248Arg) single nucleotide variant NIK deficiency [RCV001221558] Chr17:45286841 [GRCh38]
Chr17:43364208 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2728C>T (p.Arg910Cys) single nucleotide variant NIK deficiency [RCV001207399] Chr17:45264752 [GRCh38]
Chr17:43342119 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.734C>G (p.Pro245Arg) single nucleotide variant NIK deficiency [RCV001226163] Chr17:45286849 [GRCh38]
Chr17:43364216 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1190T>C (p.Val397Ala) single nucleotide variant NIK deficiency [RCV001216563] Chr17:45284912 [GRCh38]
Chr17:43362279 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.667C>T (p.Arg223Ter) single nucleotide variant NIK deficiency [RCV001201935] Chr17:45286916 [GRCh38]
Chr17:43364283 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1935G>A (p.Ala645=) single nucleotide variant NIK deficiency [RCV003106363] Chr17:45270450 [GRCh38]
Chr17:43347817 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.168G>A (p.Glu56=) single nucleotide variant NIK deficiency [RCV000929698] Chr17:45290578 [GRCh38]
Chr17:43367944 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1146C>T (p.Leu382=) single nucleotide variant NIK deficiency [RCV001453358] Chr17:45286437 [GRCh38]
Chr17:43363804 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1103G>A (p.Arg368Gln) single nucleotide variant NIK deficiency [RCV000909940] Chr17:45286480 [GRCh38]
Chr17:43363847 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1525C>A (p.Arg509=) single nucleotide variant NIK deficiency [RCV001491428] Chr17:45274150 [GRCh38]
Chr17:43351517 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1911G>A (p.Glu637=) single nucleotide variant NIK deficiency [RCV001433728] Chr17:45270474 [GRCh38]
Chr17:43347841 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1635C>T (p.Gly545=) single nucleotide variant NIK deficiency [RCV001502794] Chr17:45273525 [GRCh38]
Chr17:43350892 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.651A>G (p.Leu217=) single nucleotide variant NIK deficiency [RCV000887024] Chr17:45286932 [GRCh38]
Chr17:43364298 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1464A>G (p.Pro488=) single nucleotide variant NIK deficiency [RCV001501429] Chr17:45274211 [GRCh38]
Chr17:43351578 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-4G>C single nucleotide variant NIK deficiency [RCV000908285] Chr17:45287049 [GRCh38]
Chr17:43364415 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.989A>G (p.Lys330Arg) single nucleotide variant NIK deficiency [RCV001222706] Chr17:45286594 [GRCh38]
Chr17:43363961 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.889C>T (p.Pro297Ser) single nucleotide variant NIK deficiency [RCV001243285] Chr17:45286694 [GRCh38]
Chr17:43364061 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2485C>T (p.His829Tyr) single nucleotide variant NIK deficiency [RCV001233892] Chr17:45266630 [GRCh38]
Chr17:43343997 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.844T>C (p.Ser282Pro) single nucleotide variant NIK deficiency [RCV001066495] Chr17:45286739 [GRCh38]
Chr17:43364106 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2181T>A (p.Ser727=) single nucleotide variant not provided [RCV000934900] Chr17:45267551 [GRCh38]
Chr17:43344918 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1033G>A (p.Val345Met) single nucleotide variant NIK deficiency [RCV001046044] Chr17:45286550 [GRCh38]
Chr17:43363917 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.466C>T (p.His156Tyr) single nucleotide variant NIK deficiency [RCV001069287] Chr17:45287225 [GRCh38]
Chr17:43364591 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1098A>G (p.Arg366=) single nucleotide variant NIK deficiency [RCV001047922]|not provided [RCV003425894] Chr17:45286485 [GRCh38]
Chr17:43363852 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.1293G>A (p.Val431=) single nucleotide variant NIK deficiency [RCV001203765] Chr17:45274591 [GRCh38]
Chr17:43351958 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.2266C>T (p.Pro756Ser) single nucleotide variant NIK deficiency [RCV001212500] Chr17:45267466 [GRCh38]
Chr17:43344833 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.817C>G (p.Gln273Glu) single nucleotide variant NIK deficiency [RCV001236770] Chr17:45286766 [GRCh38]
Chr17:43364133 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2729G>A (p.Arg910His) single nucleotide variant NIK deficiency [RCV001201670] Chr17:45264751 [GRCh38]
Chr17:43342118 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.392G>A (p.Arg131His) single nucleotide variant NIK deficiency [RCV001205419] Chr17:45287299 [GRCh38]
Chr17:43364665 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.884C>T (p.Pro295Leu) single nucleotide variant NIK deficiency [RCV001205994] Chr17:45286699 [GRCh38]
Chr17:43364066 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2282G>A (p.Arg761Gln) single nucleotide variant NIK deficiency [RCV001217370] Chr17:45267450 [GRCh38]
Chr17:43344817 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1816C>T (p.Leu606Phe) single nucleotide variant NIK deficiency [RCV001228471] Chr17:45271063 [GRCh38]
Chr17:43348430 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2548C>T (p.Arg850Trp) single nucleotide variant NIK deficiency [RCV001064126] Chr17:45266567 [GRCh38]
Chr17:43343934 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.974G>A (p.Arg325His) single nucleotide variant NIK deficiency [RCV001039991] Chr17:45286609 [GRCh38]
Chr17:43363976 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.155G>A (p.Cys52Tyr) single nucleotide variant NIK deficiency [RCV001064459] Chr17:45290591 [GRCh38]
Chr17:43367957 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1489G>A (p.Gly497Ser) single nucleotide variant NIK deficiency [RCV001212473] Chr17:45274186 [GRCh38]
Chr17:43351553 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.464C>T (p.Ala155Val) single nucleotide variant NIK deficiency [RCV001202444] Chr17:45287227 [GRCh38]
Chr17:43364593 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2084C>T (p.Pro695Leu) single nucleotide variant NIK deficiency [RCV001231067] Chr17:45267648 [GRCh38]
Chr17:43345015 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2027C>T (p.Pro676Leu) single nucleotide variant NIK deficiency [RCV001216291] Chr17:45267705 [GRCh38]
Chr17:43345072 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.133G>A (p.Val45Met) single nucleotide variant NIK deficiency [RCV001056506] Chr17:45290613 [GRCh38]
Chr17:43367979 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1931C>T (p.Ala644Val) single nucleotide variant NIK deficiency [RCV001341543] Chr17:45270454 [GRCh38]
Chr17:43347821 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2176A>C (p.Lys726Gln) single nucleotide variant NIK deficiency [RCV001319914] Chr17:45267556 [GRCh38]
Chr17:43344923 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1939C>G (p.Leu647Val) single nucleotide variant NIK deficiency [RCV001340414] Chr17:45270446 [GRCh38]
Chr17:43347813 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.923A>T (p.Asp308Val) single nucleotide variant NIK deficiency [RCV001300063] Chr17:45286660 [GRCh38]
Chr17:43364027 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1244A>G (p.His415Arg) single nucleotide variant NIK deficiency [RCV001343919] Chr17:45284858 [GRCh38]
Chr17:43362225 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1821+13A>C single nucleotide variant NIK deficiency [RCV001522659]|not provided [RCV001812325] Chr17:45271045 [GRCh38]
Chr17:43348412 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.2593A>G (p.Ile865Val) single nucleotide variant NIK deficiency [RCV001314465] Chr17:45265249 [GRCh38]
Chr17:43342616 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.257-2A>G single nucleotide variant NIK deficiency [RCV001360021] Chr17:45289307 [GRCh38]
Chr17:43366673 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.717G>A (p.Val239=) single nucleotide variant NIK deficiency [RCV001294477] Chr17:45286866 [GRCh38]
Chr17:43364233 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.903G>A (p.Leu301=) single nucleotide variant NIK deficiency [RCV001397273] Chr17:45286680 [GRCh38]
Chr17:43364047 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1205A>G (p.His402Arg) single nucleotide variant NIK deficiency [RCV001344651] Chr17:45284897 [GRCh38]
Chr17:43362264 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2783C>A (p.Pro928His) single nucleotide variant NIK deficiency [RCV001323823] Chr17:45264697 [GRCh38]
Chr17:43342064 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2293G>A (p.Val765Ile) single nucleotide variant NIK deficiency [RCV001364686] Chr17:45267439 [GRCh38]
Chr17:43344806 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.653G>A (p.Arg218Gln) single nucleotide variant NIK deficiency [RCV001340598] Chr17:45286930 [GRCh38]
Chr17:43364296 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.934C>A (p.Pro312Thr) single nucleotide variant NIK deficiency [RCV001365140] Chr17:45286649 [GRCh38]
Chr17:43364016 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.214G>A (p.Glu72Lys) single nucleotide variant NIK deficiency [RCV001365317] Chr17:45290532 [GRCh38]
Chr17:43367898 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.310G>A (p.Gly104Arg) single nucleotide variant NIK deficiency [RCV001338041] Chr17:45289252 [GRCh38]
Chr17:43366618 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.977G>A (p.Gly326Asp) single nucleotide variant NIK deficiency [RCV001326832] Chr17:45286606 [GRCh38]
Chr17:43363973 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.381C>T (p.Gly127=) single nucleotide variant NIK deficiency [RCV001322627] Chr17:45287310 [GRCh38]
Chr17:43364676 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1630G>A (p.Asp544Asn) single nucleotide variant NIK deficiency [RCV001339604] Chr17:45273530 [GRCh38]
Chr17:43350897 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.934C>G (p.Pro312Ala) single nucleotide variant NIK deficiency [RCV001350340] Chr17:45286649 [GRCh38]
Chr17:43364016 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2520C>T (p.Ser840=) single nucleotide variant NIK deficiency [RCV001442142]|not provided [RCV001810605] Chr17:45266595 [GRCh38]
Chr17:43343962 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.383A>G (p.Lys128Arg) single nucleotide variant NIK deficiency [RCV001297864] Chr17:45287308 [GRCh38]
Chr17:43364674 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1225G>T (p.Gly409Cys) single nucleotide variant NIK deficiency [RCV001296578] Chr17:45284877 [GRCh38]
Chr17:43362244 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1715G>C (p.Ser572Thr) single nucleotide variant NIK deficiency [RCV001369741] Chr17:45271164 [GRCh38]
Chr17:43348531 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2579-9G>A single nucleotide variant NIK deficiency [RCV001494856] Chr17:45265272 [GRCh38]
Chr17:43342639 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2039C>T (p.Ala680Val) single nucleotide variant NIK deficiency [RCV001312810] Chr17:45267693 [GRCh38]
Chr17:43345060 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1153-9C>G single nucleotide variant NIK deficiency [RCV001359458] Chr17:45284958 [GRCh38]
Chr17:43362325 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.1803A>G (p.Arg601=) single nucleotide variant NIK deficiency [RCV001492275] Chr17:45271076 [GRCh38]
Chr17:43348443 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1203G>A (p.Thr401=) single nucleotide variant NIK deficiency [RCV001473288] Chr17:45284899 [GRCh38]
Chr17:43362266 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2579-17C>T single nucleotide variant NIK deficiency [RCV001492345] Chr17:45265280 [GRCh38]
Chr17:43342647 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.981C>T (p.Ala327=) single nucleotide variant NIK deficiency [RCV001462014] Chr17:45286602 [GRCh38]
Chr17:43363969 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.327-7G>T single nucleotide variant MAP3K14-related condition [RCV003980528]|NIK deficiency [RCV001514721] Chr17:45287371 [GRCh38]
Chr17:43364737 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.1972+17G>A single nucleotide variant NIK deficiency [RCV001498943] Chr17:45270396 [GRCh38]
Chr17:43347763 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2161C>T (p.Pro721Ser) single nucleotide variant NIK deficiency [RCV001417525] Chr17:45267571 [GRCh38]
Chr17:43344938 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-4G>A single nucleotide variant NIK deficiency [RCV001482531] Chr17:45287049 [GRCh38]
Chr17:43364415 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.306C>T (p.Ile102=) single nucleotide variant NIK deficiency [RCV001482987] Chr17:45289256 [GRCh38]
Chr17:43366622 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.765G>A (p.Thr255=) single nucleotide variant NIK deficiency [RCV001475698] Chr17:45286818 [GRCh38]
Chr17:43364185 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2754G>A (p.Ser918=) single nucleotide variant NIK deficiency [RCV001466374] Chr17:45264726 [GRCh38]
Chr17:43342093 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2433+19C>T single nucleotide variant NIK deficiency [RCV001426158] Chr17:45267073 [GRCh38]
Chr17:43344440 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2329T>C (p.Leu777=) single nucleotide variant NIK deficiency [RCV001430295] Chr17:45267196 [GRCh38]
Chr17:43344563 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1122T>C (p.Thr374=) single nucleotide variant NIK deficiency [RCV001444018] Chr17:45286461 [GRCh38]
Chr17:43363828 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1809G>A (p.Pro603=) single nucleotide variant NIK deficiency [RCV001427842] Chr17:45271070 [GRCh38]
Chr17:43348437 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.969G>C (p.Leu323=) single nucleotide variant NIK deficiency [RCV001448977] Chr17:45286614 [GRCh38]
Chr17:43363981 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1257C>T (p.Asp419=) single nucleotide variant NIK deficiency [RCV001438736] Chr17:45284845 [GRCh38]
Chr17:43362212 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2400C>T (p.Ile800=) single nucleotide variant NIK deficiency [RCV001441370] Chr17:45267125 [GRCh38]
Chr17:43344492 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2082G>A (p.Ser694=) single nucleotide variant NIK deficiency [RCV001430530] Chr17:45267650 [GRCh38]
Chr17:43345017 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1875C>T (p.Leu625=) single nucleotide variant NIK deficiency [RCV001449409] Chr17:45270510 [GRCh38]
Chr17:43347877 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1518C>T (p.Leu506=) single nucleotide variant NIK deficiency [RCV001407830] Chr17:45274157 [GRCh38]
Chr17:43351524 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2579-10C>T single nucleotide variant NIK deficiency [RCV001410932] Chr17:45265273 [GRCh38]
Chr17:43342640 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2556C>T (p.Thr852=) single nucleotide variant NIK deficiency [RCV001419332] Chr17:45266559 [GRCh38]
Chr17:43343926 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2331A>G (p.Leu777=) single nucleotide variant NIK deficiency [RCV001437953] Chr17:45267194 [GRCh38]
Chr17:43344561 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.582G>A (p.Pro194=) single nucleotide variant NIK deficiency [RCV001402817] Chr17:45287001 [GRCh38]
Chr17:43364367 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.90G>T (p.Pro30=) single nucleotide variant NIK deficiency [RCV001439258] Chr17:45290656 [GRCh38]
Chr17:43368022 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1891C>G (p.Gln631Glu) single nucleotide variant NIK deficiency [RCV001419892] Chr17:45270494 [GRCh38]
Chr17:43347861 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1291-9C>T single nucleotide variant NIK deficiency [RCV001498950] Chr17:45274602 [GRCh38]
Chr17:43351969 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-5C>T single nucleotide variant NIK deficiency [RCV001518299] Chr17:45287050 [GRCh38]
Chr17:43364416 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.1660G>T (p.Asp554Tyr) single nucleotide variant NIK deficiency [RCV001490037] Chr17:45271219 [GRCh38]
Chr17:43348586 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2298G>A (p.Pro766=) single nucleotide variant NIK deficiency [RCV001487074]|not provided [RCV003405685] Chr17:45267434 [GRCh38]
Chr17:43344801 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2511T>C (p.Ala837=) single nucleotide variant NIK deficiency [RCV001481493] Chr17:45266604 [GRCh38]
Chr17:43343971 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1359C>T (p.Val453=) single nucleotide variant NIK deficiency [RCV001490740] Chr17:45274525 [GRCh38]
Chr17:43351892 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2313G>A (p.Gln771=) single nucleotide variant NIK deficiency [RCV001406110] Chr17:45267419 [GRCh38]
Chr17:43344786 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.936C>T (p.Pro312=) single nucleotide variant NIK deficiency [RCV001475978] Chr17:45286647 [GRCh38]
Chr17:43364014 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2070G>A (p.Pro690=) single nucleotide variant NIK deficiency [RCV001500318] Chr17:45267662 [GRCh38]
Chr17:43345029 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2706C>G (p.Val902=) single nucleotide variant NIK deficiency [RCV001523210]|not provided [RCV001824990]|not specified [RCV003394113] Chr17:45264774 [GRCh38]
Chr17:43342141 [GRCh37]
Chr17:17q21.31		 benign|not provided
NM_003954.5(MAP3K14):c.656dup (p.Ala220fs) duplication NIK deficiency [RCV001523211] Chr17:45286926..45286927 [GRCh38]
Chr17:43364293..43364294 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.1822-8dup duplication NIK deficiency [RCV001484721] Chr17:45270565..45270566 [GRCh38]
Chr17:43347932..43347933 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1356T>A (p.Ile452=) single nucleotide variant NIK deficiency [RCV001434752] Chr17:45274528 [GRCh38]
Chr17:43351895 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2742G>A (p.Glu914=) single nucleotide variant NIK deficiency [RCV001397979] Chr17:45264738 [GRCh38]
Chr17:43342105 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1560C>T (p.Asn520=) single nucleotide variant NIK deficiency [RCV001423878] Chr17:45273600 [GRCh38]
Chr17:43350967 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1221C>T (p.Gly407=) single nucleotide variant NIK deficiency [RCV001489269] Chr17:45284881 [GRCh38]
Chr17:43362248 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2308C>T (p.Leu770=) single nucleotide variant NIK deficiency [RCV001484090] Chr17:45267424 [GRCh38]
Chr17:43344791 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1214G>A (p.Arg405His) single nucleotide variant NIK deficiency [RCV002001917] Chr17:45284888 [GRCh38]
Chr17:43362255 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.584A>G (p.Gln195Arg) single nucleotide variant NIK deficiency [RCV001950732] Chr17:45286999 [GRCh38]
Chr17:43364365 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1867G>A (p.Ala623Thr) single nucleotide variant NIK deficiency [RCV001950639] Chr17:45270518 [GRCh38]
Chr17:43347885 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1552+4A>G single nucleotide variant NIK deficiency [RCV001987077] Chr17:45274119 [GRCh38]
Chr17:43351486 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.775C>T (p.Pro259Ser) single nucleotide variant NIK deficiency [RCV001908580] Chr17:45286808 [GRCh38]
Chr17:43364175 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2042A>G (p.Asn681Ser) single nucleotide variant NIK deficiency [RCV001949939] Chr17:45267690 [GRCh38]
Chr17:43345057 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2144C>A (p.Pro715His) single nucleotide variant NIK deficiency [RCV001910095] Chr17:45267588 [GRCh38]
Chr17:43344955 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2530A>G (p.Met844Val) single nucleotide variant NIK deficiency [RCV001984458] Chr17:45266585 [GRCh38]
Chr17:43343952 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1152+15G>A single nucleotide variant NIK deficiency [RCV001889700] Chr17:45286416 [GRCh38]
Chr17:43363783 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2639G>A (p.Arg880Gln) single nucleotide variant NIK deficiency [RCV001945973] Chr17:45265203 [GRCh38]
Chr17:43342570 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2155C>T (p.Pro719Ser) single nucleotide variant NIK deficiency [RCV002040355] Chr17:45267577 [GRCh38]
Chr17:43344944 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2446G>T (p.Ala816Ser) single nucleotide variant NIK deficiency [RCV001910707] Chr17:45266669 [GRCh38]
Chr17:43344036 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1655C>A (p.Thr552Lys) single nucleotide variant NIK deficiency [RCV002004993] Chr17:45273505 [GRCh38]
Chr17:43350872 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.641G>A (p.Gly214Asp) single nucleotide variant NIK deficiency [RCV002020380] Chr17:45286942 [GRCh38]
Chr17:43364308 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2249C>G (p.Pro750Arg) single nucleotide variant NIK deficiency [RCV001887451] Chr17:45267483 [GRCh38]
Chr17:43344850 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.769C>T (p.Pro257Ser) single nucleotide variant NIK deficiency [RCV002035862] Chr17:45286814 [GRCh38]
Chr17:43364181 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2557G>A (p.Asp853Asn) single nucleotide variant NIK deficiency [RCV001931114] Chr17:45266558 [GRCh38]
Chr17:43343925 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2167G>A (p.Glu723Lys) single nucleotide variant NIK deficiency [RCV001979947] Chr17:45267565 [GRCh38]
Chr17:43344932 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1094C>T (p.Ser365Phe) single nucleotide variant NIK deficiency [RCV001944587] Chr17:45286489 [GRCh38]
Chr17:43363856 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1082C>T (p.Ala361Val) single nucleotide variant NIK deficiency [RCV001976870] Chr17:45286501 [GRCh38]
Chr17:43363868 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2388G>A (p.Ser796=) single nucleotide variant NIK deficiency [RCV001953599] Chr17:45267137 [GRCh38]
Chr17:43344504 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2326+5G>A single nucleotide variant NIK deficiency [RCV001999468] Chr17:45267401 [GRCh38]
Chr17:43344768 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2116A>G (p.Thr706Ala) single nucleotide variant NIK deficiency [RCV002038732] Chr17:45267616 [GRCh38]
Chr17:43344983 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1243C>T (p.His415Tyr) single nucleotide variant NIK deficiency [RCV001920039] Chr17:45284859 [GRCh38]
Chr17:43362226 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1324_1413dup (p.Met442_Leu471dup) duplication NIK deficiency [RCV001962294] Chr17:45274470..45274471 [GRCh38]
Chr17:43351837..43351838 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.884C>G (p.Pro295Arg) single nucleotide variant NIK deficiency [RCV001981920] Chr17:45286699 [GRCh38]
Chr17:43364066 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.333del (p.Glu112fs) deletion NIK deficiency [RCV002046628] Chr17:45287358 [GRCh38]
Chr17:43364724 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1657+3_1657+168del deletion NIK deficiency [RCV001930919] Chr17:45273335..45273500 [GRCh38]
Chr17:43350702..43350867 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2144C>G (p.Pro715Arg) single nucleotide variant NIK deficiency [RCV001957712] Chr17:45267588 [GRCh38]
Chr17:43344955 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.610G>A (p.Gly204Ser) single nucleotide variant NIK deficiency [RCV002049631] Chr17:45286973 [GRCh38]
Chr17:43364339 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1360C>G (p.Pro454Ala) single nucleotide variant NIK deficiency [RCV001990170] Chr17:45274524 [GRCh38]
Chr17:43351891 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1147A>G (p.Thr383Ala) single nucleotide variant NIK deficiency [RCV001922049] Chr17:45286436 [GRCh38]
Chr17:43363803 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1924G>A (p.Val642Met) single nucleotide variant NIK deficiency [RCV001978274] Chr17:45270461 [GRCh38]
Chr17:43347828 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.193G>A (p.Gly65Ser) single nucleotide variant NIK deficiency [RCV001973496] Chr17:45290553 [GRCh38]
Chr17:43367919 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1723G>A (p.Ala575Thr) single nucleotide variant NIK deficiency [RCV001972258] Chr17:45271156 [GRCh38]
Chr17:43348523 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.538-5C>A single nucleotide variant NIK deficiency [RCV001875601] Chr17:45287050 [GRCh38]
Chr17:43364416 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.916del (p.Cys306fs) deletion NIK deficiency [RCV001978448] Chr17:45286667 [GRCh38]
Chr17:43364034 [GRCh37]
Chr17:17q21.31		 likely pathogenic
NM_003954.5(MAP3K14):c.1019C>T (p.Ala340Val) single nucleotide variant NIK deficiency [RCV001925625] Chr17:45286564 [GRCh38]
Chr17:43363931 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2158G>T (p.Glu720Ter) single nucleotide variant NIK deficiency [RCV001993948] Chr17:45267574 [GRCh38]
Chr17:43344941 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.106C>G (p.Gln36Glu) single nucleotide variant NIK deficiency [RCV002029802] Chr17:45290640 [GRCh38]
Chr17:43368006 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2470C>G (p.Leu824Val) single nucleotide variant NIK deficiency [RCV001952257] Chr17:45266645 [GRCh38]
Chr17:43344012 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.485C>T (p.Ala162Val) single nucleotide variant NIK deficiency [RCV001997946] Chr17:45287206 [GRCh38]
Chr17:43364572 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.28G>C (p.Gly10Arg) single nucleotide variant NIK deficiency [RCV002026368] Chr17:45290718 [GRCh38]
Chr17:43368084 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1152+14C>T single nucleotide variant NIK deficiency [RCV002032277] Chr17:45286417 [GRCh38]
Chr17:43363784 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2206G>C (p.Glu736Gln) single nucleotide variant NIK deficiency [RCV001999152] Chr17:45267526 [GRCh38]
Chr17:43344893 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.783C>G (p.Ser261Arg) single nucleotide variant NIK deficiency [RCV001900107] Chr17:45286800 [GRCh38]
Chr17:43364167 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1901T>G (p.Leu634Arg) single nucleotide variant NIK deficiency [RCV002034115] Chr17:45270484 [GRCh38]
Chr17:43347851 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1001A>C (p.Glu334Ala) single nucleotide variant NIK deficiency [RCV001923922] Chr17:45286582 [GRCh38]
Chr17:43363949 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2797G>A (p.Ala933Thr) single nucleotide variant NIK deficiency [RCV002017913] Chr17:45264683 [GRCh38]
Chr17:43342050 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2281C>T (p.Arg761Trp) single nucleotide variant NIK deficiency [RCV001885984] Chr17:45267451 [GRCh38]
Chr17:43344818 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1973-3T>C single nucleotide variant NIK deficiency [RCV002036233] Chr17:45267762 [GRCh38]
Chr17:43345129 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.719G>T (p.Trp240Leu) single nucleotide variant NIK deficiency [RCV002027946] Chr17:45286864 [GRCh38]
Chr17:43364231 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1833G>T (p.Glu611Asp) single nucleotide variant NIK deficiency [RCV002051402] Chr17:45270552 [GRCh38]
Chr17:43347919 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.420C>G (p.Ser140Arg) single nucleotide variant NIK deficiency [RCV002050835] Chr17:45287271 [GRCh38]
Chr17:43364637 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2180C>T (p.Ser727Phe) single nucleotide variant NIK deficiency [RCV001897521] Chr17:45267552 [GRCh38]
Chr17:43344919 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1657+5G>C single nucleotide variant NIK deficiency [RCV001917212] Chr17:45273498 [GRCh38]
Chr17:43350865 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1290+19G>A single nucleotide variant NIK deficiency [RCV002092903] Chr17:45284793 [GRCh38]
Chr17:43362160 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1386G>A (p.Gly462=) single nucleotide variant NIK deficiency [RCV002125901]|not provided [RCV003408147] Chr17:45274498 [GRCh38]
Chr17:43351865 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1719C>T (p.Cys573=) single nucleotide variant NIK deficiency [RCV002129425] Chr17:45271160 [GRCh38]
Chr17:43348527 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1821+19C>A single nucleotide variant NIK deficiency [RCV002190300] Chr17:45271039 [GRCh38]
Chr17:43348406 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2461C>A (p.Arg821=) single nucleotide variant NIK deficiency [RCV002207003] Chr17:45266654 [GRCh38]
Chr17:43344021 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1479G>A (p.Leu493=) single nucleotide variant NIK deficiency [RCV002090204] Chr17:45274196 [GRCh38]
Chr17:43351563 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1822-19G>A single nucleotide variant NIK deficiency [RCV002146736] Chr17:45270582 [GRCh38]
Chr17:43347949 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.102G>A (p.Lys34=) single nucleotide variant NIK deficiency [RCV002166412] Chr17:45290644 [GRCh38]
Chr17:43368010 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1552+16C>T single nucleotide variant NIK deficiency [RCV002205366] Chr17:45274107 [GRCh38]
Chr17:43351474 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2109T>G (p.Ala703=) single nucleotide variant NIK deficiency [RCV002147794] Chr17:45267623 [GRCh38]
Chr17:43344990 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.257-20_257-19insG insertion NIK deficiency [RCV002088574] Chr17:45289324..45289325 [GRCh38]
Chr17:43366690..43366691 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2679+14G>A single nucleotide variant NIK deficiency [RCV002194110] Chr17:45265149 [GRCh38]
Chr17:43342516 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2715C>T (p.Asp905=) single nucleotide variant NIK deficiency [RCV002152462] Chr17:45264765 [GRCh38]
Chr17:43342132 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.257-19C>G single nucleotide variant NIK deficiency [RCV002084627] Chr17:45289324 [GRCh38]
Chr17:43366690 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2826G>A (p.Gln942=) single nucleotide variant NIK deficiency [RCV002072783] Chr17:45264654 [GRCh38]
Chr17:43342021 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2147C>G (p.Pro716Arg) single nucleotide variant NIK deficiency [RCV002117271] Chr17:45267585 [GRCh38]
Chr17:43344952 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1206C>T (p.His402=) single nucleotide variant NIK deficiency [RCV002175017] Chr17:45284896 [GRCh38]
Chr17:43362263 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.243C>T (p.Ile81=) single nucleotide variant NIK deficiency [RCV002213708] Chr17:45290503 [GRCh38]
Chr17:43367869 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2796C>T (p.Phe932=) single nucleotide variant NIK deficiency [RCV002087284] Chr17:45264684 [GRCh38]
Chr17:43342051 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1140C>T (p.Val380=) single nucleotide variant NIK deficiency [RCV002134722] Chr17:45286443 [GRCh38]
Chr17:43363810 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1152+19C>T single nucleotide variant NIK deficiency [RCV002212529] Chr17:45286412 [GRCh38]
Chr17:43363779 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1278C>T (p.Cys426=) single nucleotide variant NIK deficiency [RCV002078929] Chr17:45284824 [GRCh38]
Chr17:43362191 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2434-14T>C single nucleotide variant NIK deficiency [RCV002174083] Chr17:45266695 [GRCh38]
Chr17:43344062 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1413G>A (p.Leu471=) single nucleotide variant NIK deficiency [RCV002216084] Chr17:45274471 [GRCh38]
Chr17:43351838 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1657+9C>T single nucleotide variant NIK deficiency [RCV002215199] Chr17:45273494 [GRCh38]
Chr17:43350861 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1420+9C>G single nucleotide variant NIK deficiency [RCV002080130] Chr17:45274455 [GRCh38]
Chr17:43351822 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1972+16C>G single nucleotide variant NIK deficiency [RCV002107706] Chr17:45270397 [GRCh38]
Chr17:43347764 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2433+8G>A single nucleotide variant NIK deficiency [RCV002075739]|not provided [RCV002085842] Chr17:45267084 [GRCh38]
Chr17:43344451 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.711C>T (p.Asn237=) single nucleotide variant NIK deficiency [RCV002144904] Chr17:45286872 [GRCh38]
Chr17:43364239 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1290+15_1290+16del deletion NIK deficiency [RCV002150573] Chr17:45284796..45284797 [GRCh38]
Chr17:43362163..43362164 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2326+12C>T single nucleotide variant NIK deficiency [RCV002210487] Chr17:45267394 [GRCh38]
Chr17:43344761 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1972+15_1972+16insACAGCAAGGTAGGAAGAGCCCCAGC insertion NIK deficiency [RCV002155555] Chr17:45270397..45270398 [GRCh38]
Chr17:43347764..43347765 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1552+14C>T single nucleotide variant NIK deficiency [RCV002099671] Chr17:45274109 [GRCh38]
Chr17:43351476 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1962A>G (p.Ala654=) single nucleotide variant NIK deficiency [RCV002121950] Chr17:45270423 [GRCh38]
Chr17:43347790 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.138G>A (p.Glu46=) single nucleotide variant NIK deficiency [RCV002120363] Chr17:45290608 [GRCh38]
Chr17:43367974 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.87G>A (p.Thr29=) single nucleotide variant NIK deficiency [RCV002182061] Chr17:45290659 [GRCh38]
Chr17:43368025 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1695G>A (p.Pro565=) single nucleotide variant NIK deficiency [RCV002200953] Chr17:45271184 [GRCh38]
Chr17:43348551 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.537+7C>A single nucleotide variant NIK deficiency [RCV002164773] Chr17:45287147 [GRCh38]
Chr17:43364513 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1973-11C>A single nucleotide variant NIK deficiency [RCV002180858] Chr17:45267770 [GRCh38]
Chr17:43345137 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2769G>A (p.Gln923=) single nucleotide variant NIK deficiency [RCV002135347] Chr17:45264711 [GRCh38]
Chr17:43342078 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2679+11C>G single nucleotide variant NIK deficiency [RCV002199869] Chr17:45265152 [GRCh38]
Chr17:43342519 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2337C>T (p.Leu779=) single nucleotide variant NIK deficiency [RCV002083455] Chr17:45267188 [GRCh38]
Chr17:43344555 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1290+20del deletion NIK deficiency [RCV002143010] Chr17:45284792 [GRCh38]
Chr17:43362159 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1552+19G>A single nucleotide variant NIK deficiency [RCV002161671] Chr17:45274104 [GRCh38]
Chr17:43351471 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1657+11C>G single nucleotide variant NIK deficiency [RCV002143096] Chr17:45273492 [GRCh38]
Chr17:43350859 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2679+17C>T single nucleotide variant NIK deficiency [RCV002098784] Chr17:45265146 [GRCh38]
Chr17:43342513 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.1281T>C (p.Ala427=) single nucleotide variant NIK deficiency [RCV002162346] Chr17:45284821 [GRCh38]
Chr17:43362188 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2235G>A (p.Leu745=) single nucleotide variant NIK deficiency [RCV002200672] Chr17:45267497 [GRCh38]
Chr17:43344864 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2502G>A (p.Gln834=) single nucleotide variant NIK deficiency [RCV002202700] Chr17:45266613 [GRCh38]
Chr17:43343980 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1552+18C>A single nucleotide variant NIK deficiency [RCV002220075] Chr17:45274105 [GRCh38]
Chr17:43351472 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1973-11C>G single nucleotide variant NIK deficiency [RCV002199734] Chr17:45267770 [GRCh38]
Chr17:43345137 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1972+16C>T single nucleotide variant NIK deficiency [RCV002119656] Chr17:45270397 [GRCh38]
Chr17:43347764 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2694C>T (p.Ala898=) single nucleotide variant NIK deficiency [RCV002161278] Chr17:45264786 [GRCh38]
Chr17:43342153 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1578T>C (p.Asp526=) single nucleotide variant NIK deficiency [RCV002177906] Chr17:45273582 [GRCh38]
Chr17:43350949 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.741C>T (p.Asp247=) single nucleotide variant NIK deficiency [RCV002217474] Chr17:45286842 [GRCh38]
Chr17:43364209 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1809G>C (p.Pro603=) single nucleotide variant NIK deficiency [RCV002155267] Chr17:45271070 [GRCh38]
Chr17:43348437 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1821+11G>T single nucleotide variant NIK deficiency [RCV002104170] Chr17:45271047 [GRCh38]
Chr17:43348414 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2326+13G>A single nucleotide variant NIK deficiency [RCV002118157] Chr17:45267393 [GRCh38]
Chr17:43344760 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.257-17A>C single nucleotide variant NIK deficiency [RCV002099647] Chr17:45289322 [GRCh38]
Chr17:43366688 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.609A>G (p.Pro203=) single nucleotide variant NIK deficiency [RCV003112729] Chr17:45286974 [GRCh38]
Chr17:43364340 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1858C>T (p.Pro620Ser) single nucleotide variant NIK deficiency [RCV003116185] Chr17:45270527 [GRCh38]
Chr17:43347894 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1102C>T (p.Arg368Trp) single nucleotide variant NIK deficiency [RCV003117332] Chr17:45286481 [GRCh38]
Chr17:43363848 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.580C>T (p.Pro194Ser) single nucleotide variant NIK deficiency [RCV002295821] Chr17:45287003 [GRCh38]
Chr17:43364369 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2722C>T (p.Pro908Ser) single nucleotide variant NIK deficiency [RCV002296423] Chr17:45264758 [GRCh38]
Chr17:43342125 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1152+4A>G single nucleotide variant NIK deficiency [RCV003032863] Chr17:45286427 [GRCh38]
Chr17:43363794 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2081C>T (p.Ser694Leu) single nucleotide variant NIK deficiency [RCV002771152] Chr17:45267651 [GRCh38]
Chr17:43345018 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2327-20T>A single nucleotide variant NIK deficiency [RCV002774844] Chr17:45267218 [GRCh38]
Chr17:43344585 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1294C>T (p.Arg432Trp) single nucleotide variant not provided [RCV002511873] Chr17:45274590 [GRCh38]
Chr17:43351957 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1000G>A (p.Glu334Lys) single nucleotide variant NIK deficiency [RCV002794908] Chr17:45286583 [GRCh38]
Chr17:43363950 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1928C>G (p.Ser643Cys) single nucleotide variant NIK deficiency [RCV002971641] Chr17:45270457 [GRCh38]
Chr17:43347824 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2183C>T (p.Pro728Leu) single nucleotide variant NIK deficiency [RCV003016112] Chr17:45267549 [GRCh38]
Chr17:43344916 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.34C>T (p.Pro12Ser) single nucleotide variant NIK deficiency [RCV002858112] Chr17:45290712 [GRCh38]
Chr17:43368078 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2519C>T (p.Ser840Phe) single nucleotide variant Inborn genetic diseases [RCV002753079] Chr17:45266596 [GRCh38]
Chr17:43343963 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.538-9C>G single nucleotide variant MAP3K14-related condition [RCV003898567]|NIK deficiency [RCV002907817] Chr17:45287054 [GRCh38]
Chr17:43364420 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2033A>G (p.Asn678Ser) single nucleotide variant NIK deficiency [RCV003011709] Chr17:45267699 [GRCh38]
Chr17:43345066 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1337G>A (p.Gly446Glu) single nucleotide variant NIK deficiency [RCV003076274] Chr17:45274547 [GRCh38]
Chr17:43351914 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.334G>A (p.Glu112Lys) single nucleotide variant NIK deficiency [RCV002623092] Chr17:45287357 [GRCh38]
Chr17:43364723 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1152+12C>T single nucleotide variant NIK deficiency [RCV003003026] Chr17:45286419 [GRCh38]
Chr17:43363786 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1821+10G>A single nucleotide variant NIK deficiency [RCV002638985] Chr17:45271048 [GRCh38]
Chr17:43348415 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.200C>A (p.Ala67Asp) single nucleotide variant NIK deficiency [RCV003039408] Chr17:45290546 [GRCh38]
Chr17:43367912 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.440AGA[2] (p.Lys149del) microsatellite NIK deficiency [RCV002662751] Chr17:45287243..45287245 [GRCh38]
Chr17:43364609..43364611 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1857A>T (p.Pro619=) single nucleotide variant NIK deficiency [RCV002976608] Chr17:45270528 [GRCh38]
Chr17:43347895 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2326+20C>T single nucleotide variant NIK deficiency [RCV003035821] Chr17:45267386 [GRCh38]
Chr17:43344753 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2549G>A (p.Arg850Gln) single nucleotide variant NIK deficiency [RCV002912831] Chr17:45266566 [GRCh38]
Chr17:43343933 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1152+11C>T single nucleotide variant NIK deficiency [RCV002820585] Chr17:45286420 [GRCh38]
Chr17:43363787 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.89C>T (p.Pro30Leu) single nucleotide variant NIK deficiency [RCV002637031] Chr17:45290657 [GRCh38]
Chr17:43368023 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.537+15C>T single nucleotide variant NIK deficiency [RCV002949243] Chr17:45287139 [GRCh38]
Chr17:43364505 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1818C>T (p.Leu606=) single nucleotide variant NIK deficiency [RCV002736382] Chr17:45271061 [GRCh38]
Chr17:43348428 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2387C>T (p.Ser796Leu) single nucleotide variant NIK deficiency [RCV002927650] Chr17:45267138 [GRCh38]
Chr17:43344505 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1735G>A (p.Val579Ile) single nucleotide variant NIK deficiency [RCV003036894] Chr17:45271144 [GRCh38]
Chr17:43348511 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1569G>T (p.Leu523=) single nucleotide variant NIK deficiency [RCV002885716] Chr17:45273591 [GRCh38]
Chr17:43350958 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2547dup (p.Arg850fs) duplication NIK deficiency [RCV002847917] Chr17:45266567..45266568 [GRCh38]
Chr17:43343934..43343935 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1821+3C>G single nucleotide variant NIK deficiency [RCV002761511] Chr17:45271055 [GRCh38]
Chr17:43348422 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2627G>A (p.Arg876Gln) single nucleotide variant NIK deficiency [RCV003054196] Chr17:45265215 [GRCh38]
Chr17:43342582 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1233C>T (p.Phe411=) single nucleotide variant NIK deficiency [RCV002954088] Chr17:45284869 [GRCh38]
Chr17:43362236 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2529C>T (p.Asn843=) single nucleotide variant NIK deficiency [RCV002895035] Chr17:45266586 [GRCh38]
Chr17:43343953 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1821+9C>T single nucleotide variant NIK deficiency [RCV003085557] Chr17:45271049 [GRCh38]
Chr17:43348416 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.2301G>T (p.Glu767Asp) single nucleotide variant NIK deficiency [RCV003023539] Chr17:45267431 [GRCh38]
Chr17:43344798 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1777T>C (p.Cys593Arg) single nucleotide variant NIK deficiency [RCV002800703] Chr17:45271102 [GRCh38]
Chr17:43348469 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2433+16C>T single nucleotide variant NIK deficiency [RCV002711531] Chr17:45267076 [GRCh38]
Chr17:43344443 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.320A>G (p.Gln107Arg) single nucleotide variant NIK deficiency [RCV002957356] Chr17:45289242 [GRCh38]
Chr17:43366608 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.436C>A (p.Arg146=) single nucleotide variant NIK deficiency [RCV002765583] Chr17:45287255 [GRCh38]
Chr17:43364621 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.859C>T (p.Leu287=) single nucleotide variant NIK deficiency [RCV002958614] Chr17:45286724 [GRCh38]
Chr17:43364091 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.2482G>A (p.Val828Ile) single nucleotide variant NIK deficiency [RCV002766618] Chr17:45266633 [GRCh38]
Chr17:43344000 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1797C>A (p.Phe599Leu) single nucleotide variant NIK deficiency [RCV003005759] Chr17:45271082 [GRCh38]
Chr17:43348449 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1048G>C (p.Ala350Pro) single nucleotide variant NIK deficiency [RCV003025205] Chr17:45286535 [GRCh38]
Chr17:43363902 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.41C>T (p.Ser14Leu) single nucleotide variant NIK deficiency [RCV003084542] Chr17:45290705 [GRCh38]
Chr17:43368071 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.735C>T (p.Pro245=) single nucleotide variant NIK deficiency [RCV003056623] Chr17:45286848 [GRCh38]
Chr17:43364215 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.188C>A (p.Thr63Asn) single nucleotide variant NIK deficiency [RCV002625630] Chr17:45290558 [GRCh38]
Chr17:43367924 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1573A>C (p.Ser525Arg) single nucleotide variant NIK deficiency [RCV002982312] Chr17:45273587 [GRCh38]
Chr17:43350954 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2555C>T (p.Thr852Ile) single nucleotide variant Inborn genetic diseases [RCV002764543] Chr17:45266560 [GRCh38]
Chr17:43343927 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.61_73del (p.Glu21fs) deletion NIK deficiency [RCV002876337] Chr17:45290673..45290685 [GRCh38]
Chr17:43368039..43368051 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2823C>T (p.Gly941=) single nucleotide variant NIK deficiency [RCV003056272] Chr17:45264657 [GRCh38]
Chr17:43342024 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1958G>A (p.Arg653Gln) single nucleotide variant NIK deficiency [RCV003081914] Chr17:45270427 [GRCh38]
Chr17:43347794 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1821G>A (p.Lys607=) single nucleotide variant NIK deficiency [RCV003048991] Chr17:45271058 [GRCh38]
Chr17:43348425 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.162G>A (p.Lys54=) single nucleotide variant NIK deficiency [RCV002650779] Chr17:45290584 [GRCh38]
Chr17:43367950 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2146C>G (p.Pro716Ala) single nucleotide variant Inborn genetic diseases [RCV002854886] Chr17:45267586 [GRCh38]
Chr17:43344953 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1290+4C>T single nucleotide variant NIK deficiency [RCV002933595] Chr17:45284808 [GRCh38]
Chr17:43362175 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1575C>T (p.Ser525=) single nucleotide variant NIK deficiency [RCV002628261] Chr17:45273585 [GRCh38]
Chr17:43350952 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2437C>A (p.Pro813Thr) single nucleotide variant NIK deficiency [RCV003088901] Chr17:45266678 [GRCh38]
Chr17:43344045 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2131C>T (p.Pro711Ser) single nucleotide variant NIK deficiency [RCV002577279] Chr17:45267601 [GRCh38]
Chr17:43344968 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1881C>T (p.Ala627=) single nucleotide variant NIK deficiency [RCV002833282] Chr17:45270504 [GRCh38]
Chr17:43347871 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.295C>T (p.Arg99Cys) single nucleotide variant NIK deficiency [RCV002933579] Chr17:45289267 [GRCh38]
Chr17:43366633 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2576A>G (p.Asn859Ser) single nucleotide variant NIK deficiency [RCV002806235] Chr17:45266539 [GRCh38]
Chr17:43343906 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.458C>A (p.Ser153Tyr) single nucleotide variant NIK deficiency [RCV003030045] Chr17:45287233 [GRCh38]
Chr17:43364599 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2248C>G (p.Pro750Ala) single nucleotide variant Inborn genetic diseases [RCV002769768] Chr17:45267484 [GRCh38]
Chr17:43344851 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2690C>G (p.Ala897Gly) single nucleotide variant NIK deficiency [RCV002811882] Chr17:45264790 [GRCh38]
Chr17:43342157 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.822C>T (p.Pro274=) single nucleotide variant NIK deficiency [RCV002650035] Chr17:45286761 [GRCh38]
Chr17:43364128 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.215A>C (p.Glu72Ala) single nucleotide variant NIK deficiency [RCV002651329] Chr17:45290531 [GRCh38]
Chr17:43367897 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1802G>A (p.Arg601Gln) single nucleotide variant NIK deficiency [RCV003060946] Chr17:45271077 [GRCh38]
Chr17:43348444 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.326+13G>A single nucleotide variant NIK deficiency [RCV002857593] Chr17:45289223 [GRCh38]
Chr17:43366589 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.257-16A>C single nucleotide variant NIK deficiency [RCV002653754] Chr17:45289321 [GRCh38]
Chr17:43366687 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2679+6G>T single nucleotide variant NIK deficiency [RCV003071594] Chr17:45265157 [GRCh38]
Chr17:43342524 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2288C>G (p.Ala763Gly) single nucleotide variant NIK deficiency [RCV002654873] Chr17:45267444 [GRCh38]
Chr17:43344811 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1708G>T (p.Gly570Cys) single nucleotide variant NIK deficiency [RCV003052089] Chr17:45271171 [GRCh38]
Chr17:43348538 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.836C>T (p.Pro279Leu) single nucleotide variant NIK deficiency [RCV003093786] Chr17:45286747 [GRCh38]
Chr17:43364114 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2433+18C>T single nucleotide variant NIK deficiency [RCV002610876] Chr17:45267074 [GRCh38]
Chr17:43344441 [GRCh37]
Chr17:17q21.31		 likely benign|uncertain significance
NM_003954.5(MAP3K14):c.1602C>T (p.Asp534=) single nucleotide variant NIK deficiency [RCV003068314] Chr17:45273558 [GRCh38]
Chr17:43350925 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.1545C>T (p.Asp515=) single nucleotide variant NIK deficiency [RCV002944280] Chr17:45274130 [GRCh38]
Chr17:43351497 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.428G>A (p.Arg143Gln) single nucleotide variant NIK deficiency [RCV003050829] Chr17:45287263 [GRCh38]
Chr17:43364629 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2436C>A (p.Asn812Lys) single nucleotide variant Inborn genetic diseases [RCV003357949] Chr17:45266679 [GRCh38]
Chr17:43344046 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2094A>G (p.Pro698=) single nucleotide variant NIK deficiency [RCV003875108] Chr17:45267638 [GRCh38]
Chr17:43345005 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2434-25C>T single nucleotide variant not specified [RCV003391183] Chr17:45266706 [GRCh38]
Chr17:43344073 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.1291-89G>A single nucleotide variant not specified [RCV003397164] Chr17:45274682 [GRCh38]
Chr17:43352049 [GRCh37]
Chr17:17q21.31		 benign
NM_003954.5(MAP3K14):c.2434-7G>A single nucleotide variant NIK deficiency [RCV003879068] Chr17:45266688 [GRCh38]
Chr17:43344055 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-10C>T single nucleotide variant NIK deficiency [RCV003878314] Chr17:45287055 [GRCh38]
Chr17:43364421 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.816C>T (p.Leu272=) single nucleotide variant NIK deficiency [RCV003881910] Chr17:45286767 [GRCh38]
Chr17:43364134 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2832G>A (p.Glu944=) single nucleotide variant NIK deficiency [RCV003593647] Chr17:45264648 [GRCh38]
Chr17:43342015 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1658-12C>A single nucleotide variant NIK deficiency [RCV003595078] Chr17:45271233 [GRCh38]
Chr17:43348600 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.477G>C (p.Val159=) single nucleotide variant NIK deficiency [RCV003595145] Chr17:45287214 [GRCh38]
Chr17:43364580 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1134G>A (p.Glu378=) single nucleotide variant NIK deficiency [RCV003595321] Chr17:45286449 [GRCh38]
Chr17:43363816 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.213C>T (p.Ser71=) single nucleotide variant NIK deficiency [RCV003595373] Chr17:45290533 [GRCh38]
Chr17:43367899 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1421-15C>T single nucleotide variant NIK deficiency [RCV003595481] Chr17:45274269 [GRCh38]
Chr17:43351636 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2460G>T (p.Ser820=) single nucleotide variant NIK deficiency [RCV003594489] Chr17:45266655 [GRCh38]
Chr17:43344022 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2175C>T (p.Asn725=) single nucleotide variant NIK deficiency [RCV003594516] Chr17:45267557 [GRCh38]
Chr17:43344924 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2481C>T (p.Gly827=) single nucleotide variant NIK deficiency [RCV003594751] Chr17:45266634 [GRCh38]
Chr17:43344001 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2247G>A (p.Glu749=) single nucleotide variant NIK deficiency [RCV003594855] Chr17:45267485 [GRCh38]
Chr17:43344852 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-8C>G single nucleotide variant NIK deficiency [RCV003595129] Chr17:45287053 [GRCh38]
Chr17:43364419 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.997G>A (p.Val333Met) single nucleotide variant NIK deficiency [RCV003594535] Chr17:45286586 [GRCh38]
Chr17:43363953 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2028G>A (p.Pro676=) single nucleotide variant NIK deficiency [RCV003815901] Chr17:45267704 [GRCh38]
Chr17:43345071 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1467G>A (p.Glu489=) single nucleotide variant NIK deficiency [RCV003594755] Chr17:45274208 [GRCh38]
Chr17:43351575 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1658-9C>T single nucleotide variant NIK deficiency [RCV003855685] Chr17:45271230 [GRCh38]
Chr17:43348597 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1002G>A (p.Glu334=) single nucleotide variant NIK deficiency [RCV003595377] Chr17:45286581 [GRCh38]
Chr17:43363948 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1902G>A (p.Leu634=) single nucleotide variant NIK deficiency [RCV003594523] Chr17:45270483 [GRCh38]
Chr17:43347850 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1180C>A (p.Arg394=) single nucleotide variant NIK deficiency [RCV003838705] Chr17:45284922 [GRCh38]
Chr17:43362289 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1443C>G (p.Val481=) single nucleotide variant NIK deficiency [RCV003761123] Chr17:45274232 [GRCh38]
Chr17:43351599 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2460G>A (p.Ser820=) single nucleotide variant NIK deficiency [RCV003594772] Chr17:45266655 [GRCh38]
Chr17:43344022 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2193T>A (p.Thr731=) single nucleotide variant NIK deficiency [RCV003831991] Chr17:45267539 [GRCh38]
Chr17:43344906 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.885C>T (p.Pro295=) single nucleotide variant NIK deficiency [RCV003595408] Chr17:45286698 [GRCh38]
Chr17:43364065 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1066C>T (p.Leu356=) single nucleotide variant NIK deficiency [RCV003761144] Chr17:45286517 [GRCh38]
Chr17:43363884 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2327-20T>C single nucleotide variant NIK deficiency [RCV003850051] Chr17:45267218 [GRCh38]
Chr17:43344585 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.24C>T (p.Cys8=) single nucleotide variant NIK deficiency [RCV003759933] Chr17:45290722 [GRCh38]
Chr17:43368088 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.537+16C>T single nucleotide variant NIK deficiency [RCV003759203] Chr17:45287138 [GRCh38]
Chr17:43364504 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.546G>A (p.Glu182=) single nucleotide variant NIK deficiency [RCV003759346] Chr17:45287037 [GRCh38]
Chr17:43364403 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2760C>T (p.Ile920=) single nucleotide variant NIK deficiency [RCV003861227] Chr17:45264720 [GRCh38]
Chr17:43342087 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1875C>G (p.Leu625=) single nucleotide variant NIK deficiency [RCV003759508] Chr17:45270510 [GRCh38]
Chr17:43347877 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2184T>C (p.Pro728=) single nucleotide variant NIK deficiency [RCV003760580] Chr17:45267548 [GRCh38]
Chr17:43344915 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1707G>T (p.Leu569=) single nucleotide variant NIK deficiency [RCV003760570] Chr17:45271172 [GRCh38]
Chr17:43348539 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.861G>T (p.Leu287=) single nucleotide variant NIK deficiency [RCV003759608] Chr17:45286722 [GRCh38]
Chr17:43364089 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2289A>G (p.Ala763=) single nucleotide variant MAP3K14-related condition [RCV003941468] Chr17:45267443 [GRCh38]
Chr17:43344810 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.714C>T (p.His238=) single nucleotide variant NIK deficiency [RCV003760248] Chr17:45286869 [GRCh38]
Chr17:43364236 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1553-11C>T single nucleotide variant NIK deficiency [RCV003859829] Chr17:45273618 [GRCh38]
Chr17:43350985 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.579C>T (p.Thr193=) single nucleotide variant NIK deficiency [RCV003870053] Chr17:45287004 [GRCh38]
Chr17:43364370 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.735C>G (p.Pro245=) single nucleotide variant NIK deficiency [RCV003868918] Chr17:45286848 [GRCh38]
Chr17:43364215 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-13T>C single nucleotide variant NIK deficiency [RCV003759480] Chr17:45287058 [GRCh38]
Chr17:43364424 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.652C>T (p.Arg218Trp) single nucleotide variant NIK deficiency [RCV003846238] Chr17:45286931 [GRCh38]
Chr17:43364297 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.747C>G (p.Gly249=) single nucleotide variant NIK deficiency [RCV003760138] Chr17:45286836 [GRCh38]
Chr17:43364203 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2553C>G (p.Pro851=) single nucleotide variant NIK deficiency [RCV003758391] Chr17:45266562 [GRCh38]
Chr17:43343929 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.561C>A (p.Ala187=) single nucleotide variant NIK deficiency [RCV003760270] Chr17:45287022 [GRCh38]
Chr17:43364388 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.90G>A (p.Pro30=) single nucleotide variant NIK deficiency [RCV003760471] Chr17:45290656 [GRCh38]
Chr17:43368022 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1839G>A (p.Pro613=) single nucleotide variant NIK deficiency [RCV003760483] Chr17:45270546 [GRCh38]
Chr17:43347913 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.2700C>T (p.Ser900=) single nucleotide variant NIK deficiency [RCV003760701] Chr17:45264780 [GRCh38]
Chr17:43342147 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1761G>T (p.Leu587=) single nucleotide variant NIK deficiency [RCV003760749] Chr17:45271118 [GRCh38]
Chr17:43348485 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1250T>A (p.Met417Lys) single nucleotide variant NIK deficiency [RCV003759242] Chr17:45284852 [GRCh38]
Chr17:43362219 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_003954.5(MAP3K14):c.2727T>A (p.Val909=) single nucleotide variant NIK deficiency [RCV003759509] Chr17:45264753 [GRCh38]
Chr17:43342120 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1569G>A (p.Leu523=) single nucleotide variant NIK deficiency [RCV003759638] Chr17:45273591 [GRCh38]
Chr17:43350958 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.538-17T>A single nucleotide variant NIK deficiency [RCV003841435] Chr17:45287062 [GRCh38]
Chr17:43364428 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1890C>G (p.Ile630Met) single nucleotide variant MAP3K14-related condition [RCV003944436] Chr17:45270495 [GRCh38]
Chr17:43347862 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.816C>G (p.Leu272=) single nucleotide variant MAP3K14-related condition [RCV003944133] Chr17:45286767 [GRCh38]
Chr17:43364134 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1647C>T (p.Ser549=) single nucleotide variant MAP3K14-related condition [RCV003983716] Chr17:45273513 [GRCh38]
Chr17:43350880 [GRCh37]
Chr17:17q21.31		 likely benign
NM_003954.5(MAP3K14):c.1008C>T (p.Tyr336=) single nucleotide variant MAP3K14-related condition [RCV003969350] Chr17:45286575 [GRCh38]
Chr17:43363942 [GRCh37]
Chr17:17q21.31		 likely benign
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR31hsa-miR-31-5pOncomiRDBexternal_infoNANA22264793
MIR155hsa-miR-155-5pMirtarbaseexternal_infoReporter assayFunctional MTI20584899

Predicted Target Of
Summary Value
Count of predictions:1597
Count of miRNA genes:482
Interacting mature miRNAs:520
Transcripts:ENST00000344686, ENST00000376926, ENST00000586644, ENST00000587332, ENST00000592267
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
STS-Y10256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371743,341,813 - 43,342,014UniSTSGRCh37
Build 361740,697,596 - 40,697,797RGDNCBI36
Celera1740,051,180 - 40,051,381RGD
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
HuRef1739,102,580 - 39,102,781UniSTS
GeneMap99-GB4 RH Map17329.87UniSTS
NCBI RH Map17577.7UniSTS
STS-D29513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371743,340,616 - 43,340,863UniSTSGRCh37
Build 361740,696,399 - 40,696,646RGDNCBI36
Celera1740,049,983 - 40,050,230RGD
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
HuRef1739,101,383 - 39,101,630UniSTS
GeneMap99-GB4 RH Map17329.72UniSTS
NCBI RH Map17581.8UniSTS
RH92291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371743,355,041 - 43,355,180UniSTSGRCh37
Build 361740,710,824 - 40,710,963RGDNCBI36
Celera1740,064,408 - 40,064,547RGD
Cytogenetic Map17q21UniSTS
HuRef1739,115,808 - 39,115,947UniSTS
GeneMap99-GB4 RH Map17329.72UniSTS
MAP3K14_912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371743,340,400 - 43,341,144UniSTSGRCh37
Build 361740,696,183 - 40,696,927RGDNCBI36
Celera1740,049,767 - 40,050,511RGD
HuRef1739,101,167 - 39,101,911UniSTS
RH15917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371743,346,962 - 43,347,130UniSTSGRCh37
Build 361740,702,745 - 40,702,913RGDNCBI36
Celera1740,056,329 - 40,056,497RGD
Cytogenetic Map17q21UniSTS
HuRef1739,107,729 - 39,107,897UniSTS
GeneMap99-GB4 RH Map17329.72UniSTS
NCBI RH Map17581.6UniSTS
SHGC-32453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371743,340,502 - 43,340,651UniSTSGRCh37
Build 361740,696,285 - 40,696,434RGDNCBI36
Celera1740,049,869 - 40,050,018RGD
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
HuRef1739,101,269 - 39,101,418UniSTS
Stanford-G3 RH Map171928.0UniSTS
Whitehead-RH Map17356.4UniSTS
NCBI RH Map17587.8UniSTS
GeneMap99-G3 RH Map172429.0UniSTS
D10S512  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17q21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
D10S16   No map positions available.
D15S1477  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q32-q35UniSTS
Cytogenetic Map5q11UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map2q31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map1q31.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map3p25-p24UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map3p12UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map14q11.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p22.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map15q21-q23UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map17qUniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map6p24.2UniSTS
G44334  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q21UniSTS
L17971  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q21UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic MapXq22UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map20p11.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map9q34.13UniSTS
D1S1361  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p21.1-p12.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map17q21UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS
L17877  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map9q21.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map17q25.3UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
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Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1955 887 947 221 1404 111 3017 1541 1463 213 1249 1295 125 828 1978 1 1
Low 484 2102 779 403 545 354 1339 656 2270 206 211 318 50 1 376 810 5 1
Below cutoff 2 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_033823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011525441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436998 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_934591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA564389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC003070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC003963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC008105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ008163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK131438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE645094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU623799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA856801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ314874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY096069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY287427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT585122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y10256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000344686   ⟹   ENSP00000478552
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1745,263,119 - 45,317,020 (-)Ensembl
RefSeq Acc Id: ENST00000376926   ⟹   ENSP00000482657
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1745,263,128 - 45,290,976 (-)Ensembl
RefSeq Acc Id: ENST00000586644
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1745,263,151 - 45,273,602 (-)Ensembl
RefSeq Acc Id: ENST00000592267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1745,263,135 - 45,273,966 (-)Ensembl
RefSeq Acc Id: ENST00000617331   ⟹   ENSP00000480974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1745,264,636 - 45,317,029 (-)Ensembl
RefSeq Acc Id: ENST00000680632   ⟹   ENSP00000505027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1745,263,128 - 45,284,949 (-)Ensembl
RefSeq Acc Id: NM_003954   ⟹   NP_003945
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,263,119 - 45,317,020 (-)NCBI
GRCh371743,340,488 - 43,394,414 (-)ENTREZGENE
Build 361740,696,271 - 40,750,197 (-)NCBI Archive
HuRef1739,101,255 - 39,155,179 (-)ENTREZGENE
CHM1_11743,575,750 - 43,629,737 (-)NCBI
T2T-CHM13v2.01746,116,902 - 46,170,784 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011525441   ⟹   XP_011523743
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,263,119 - 45,317,020 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047436997   ⟹   XP_047292953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,263,119 - 45,317,020 (-)NCBI
RefSeq Acc Id: XM_047436998   ⟹   XP_047292954
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,263,119 - 45,317,020 (-)NCBI
RefSeq Acc Id: XM_054317683   ⟹   XP_054173658
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01746,116,902 - 46,170,784 (-)NCBI
RefSeq Acc Id: XM_054317684   ⟹   XP_054173659
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01746,116,902 - 46,170,784 (-)NCBI
RefSeq Acc Id: XM_054317685   ⟹   XP_054173660
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01746,116,902 - 46,170,784 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_003945   ⟸   NM_003954
- UniProtKB: D3DX67 (UniProtKB/Swiss-Prot),   A8K2D8 (UniProtKB/Swiss-Prot),   Q8IYN1 (UniProtKB/Swiss-Prot),   Q99558 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011523743   ⟸   XM_011525441
- Peptide Label: isoform X2
- UniProtKB: D3DX67 (UniProtKB/Swiss-Prot),   A8K2D8 (UniProtKB/Swiss-Prot),   Q8IYN1 (UniProtKB/Swiss-Prot),   Q99558 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000482657   ⟸   ENST00000376926
RefSeq Acc Id: ENSP00000480974   ⟸   ENST00000617331
RefSeq Acc Id: ENSP00000478552   ⟸   ENST00000344686
RefSeq Acc Id: ENSP00000505027   ⟸   ENST00000680632
RefSeq Acc Id: XP_047292953   ⟸   XM_047436997
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047292954   ⟸   XM_047436998
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054173658   ⟸   XM_054317683
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054173660   ⟸   XM_054317685
- Peptide Label: isoform X2
- UniProtKB: Q99558 (UniProtKB/Swiss-Prot),   D3DX67 (UniProtKB/Swiss-Prot),   A8K2D8 (UniProtKB/Swiss-Prot),   Q8IYN1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054173659   ⟸   XM_054317684
- Peptide Label: isoform X1
Protein Domains
Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q99558-F1-model_v2 AlphaFold Q99558 1-947 view protein structure

Promoters
RGD ID:6794302
Promoter ID:HG_KWN:26369
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:UC002IIU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361740,706,756 - 40,707,477 (-)MPROMDB
RGD ID:6794304
Promoter ID:HG_KWN:26370
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000376926,   UC010DAJ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361740,719,456 - 40,719,956 (-)MPROMDB
RGD ID:6794301
Promoter ID:HG_KWN:26371
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:UC002IIV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361740,723,871 - 40,724,371 (-)MPROMDB
RGD ID:6794300
Promoter ID:HG_KWN:26372
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000344686,   NM_003954
Position:
Human AssemblyChrPosition (strand)Source
Build 361740,750,051 - 40,750,697 (-)MPROMDB
RGD ID:7235331
Promoter ID:EPDNEW_H23411
Type:multiple initiation site
Name:MAP3K14_2
Description:mitogen-activated protein kinase kinase kinase 14
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23412  EPDNEW_H23413  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,290,956 - 45,291,016EPDNEW
RGD ID:7235333
Promoter ID:EPDNEW_H23412
Type:initiation region
Name:MAP3K14_1
Description:mitogen-activated protein kinase kinase kinase 14
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23411  EPDNEW_H23413  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,317,017 - 45,317,077EPDNEW
RGD ID:7235335
Promoter ID:EPDNEW_H23413
Type:initiation region
Name:MAP3K14_3
Description:mitogen-activated protein kinase kinase kinase 14
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23411  EPDNEW_H23412  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381745,317,145 - 45,317,205EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6853 AgrOrtholog
COSMIC MAP3K14 COSMIC
Ensembl Genes ENSG00000006062 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000344686 ENTREZGENE
  ENST00000344686.8 UniProtKB/Swiss-Prot
  ENST00000376926.8 UniProtKB/Swiss-Prot
  ENST00000617331 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000617331.3 UniProtKB/Swiss-Prot
  ENST00000680632.1 UniProtKB/TrEMBL
Gene3D-CATH Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000006062 GTEx
HGNC ID HGNC:6853 ENTREZGENE
Human Proteome Map MAP3K14 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  M3K14_STKc UniProtKB/Swiss-Prot
  MAPKKK14 UniProtKB/Swiss-Prot
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9020 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 9020 ENTREZGENE
OMIM 604655 OMIM
PANTHER MAP KINASE KINASE KINASE SSK2-RELATED-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR48016:SF9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30597 PharmGKB
PIRSF MAPKKK14 UniProtKB/Swiss-Prot
PROSITE PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WXF1_HUMAN UniProtKB/TrEMBL
  A0A7P0Z419_HUMAN UniProtKB/TrEMBL
  A8K2D8 ENTREZGENE
  D3DX67 ENTREZGENE
  M3K14_HUMAN UniProtKB/Swiss-Prot
  Q68D39_HUMAN UniProtKB/TrEMBL
  Q8IYN1 ENTREZGENE
  Q99558 ENTREZGENE
UniProt Secondary A8K2D8 UniProtKB/Swiss-Prot
  D3DX67 UniProtKB/Swiss-Prot
  Q8IYN1 UniProtKB/Swiss-Prot