TRIOBP (TRIO and F-actin binding protein) - Rat Genome Database

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Gene: TRIOBP (TRIO and F-actin binding protein) Homo sapiens
Analyze
Symbol: TRIOBP
Name: TRIO and F-actin binding protein
RGD ID: 1605399
HGNC Page HGNC
Description: Enables actin filament binding activity and ubiquitin protein ligase binding activity. Acts upstream of or within positive regulation of substrate adhesion-dependent cell spreading. Located in actin cytoskeleton. Implicated in autosomal recessive nonsyndromic deafness 28.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: deafness, autosomal recessive 28; DFNB28; dJ37E16.4; FLJ39315; HRIHFB2122; KIAA1662; TAP68; TARA; tara-like protein; TRIO and F-actin-binding protein; trio-associated repeat on actin
RGD Orthologs
Mouse
Rat
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
GRCh38.p13 Ensembl2237,697,048 - 37,776,556 (+)EnsemblGRCh38hg38GRCh38
GRCh382237,697,048 - 37,776,556 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372238,093,055 - 38,172,563 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362236,423,574 - 36,502,509 (+)NCBINCBI36hg18NCBI36
Celera2221,894,838 - 21,974,375 (+)NCBI
Cytogenetic Map22q13.1NCBI
HuRef2221,059,927 - 21,139,806 (+)NCBIHuRef
CHM1_12238,051,700 - 38,131,297 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:8500161   PMID:8889548   PMID:9853615   PMID:10591208   PMID:11076863   PMID:11148140   PMID:11258795   PMID:12168954   PMID:12477932   PMID:14702039   PMID:15489334   PMID:15489336  
PMID:16169070   PMID:16344560   PMID:16381901   PMID:16385457   PMID:16385458   PMID:17081983   PMID:17629495   PMID:18029348   PMID:18194665   PMID:19322201   PMID:19913121   PMID:19996280  
PMID:20301607   PMID:20360068   PMID:20628086   PMID:21423176   PMID:21873635   PMID:21988832   PMID:22820163   PMID:24692559   PMID:25130170   PMID:25333879   PMID:25900982   PMID:26186194  
PMID:26344197   PMID:26496610   PMID:27197753   PMID:27546710   PMID:27764096   PMID:27880917   PMID:28089734   PMID:28330616   PMID:28438837   PMID:28514442   PMID:28611215   PMID:28977470  
PMID:29197352   PMID:29507111   PMID:29509190   PMID:29568061   PMID:29669786   PMID:29890989   PMID:30196744   PMID:30344098   PMID:30471916   PMID:30472188   PMID:30833792   PMID:30979931  
PMID:31527615   PMID:31586073   PMID:31815665   PMID:33957083   PMID:34079125  


Genomics

Comparative Map Data
TRIOBP
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2237,697,048 - 37,776,556 (+)EnsemblGRCh38hg38GRCh38
GRCh382237,697,048 - 37,776,556 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372238,093,055 - 38,172,563 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362236,423,574 - 36,502,509 (+)NCBINCBI36hg18NCBI36
Celera2221,894,838 - 21,974,375 (+)NCBI
Cytogenetic Map22q13.1NCBI
HuRef2221,059,927 - 21,139,806 (+)NCBIHuRef
CHM1_12238,051,700 - 38,131,297 (+)NCBICHM1_1
Triobp
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391578,831,924 - 78,890,069 (+)NCBIGRCm39mm39
GRCm39 Ensembl1578,831,924 - 78,890,069 (+)Ensembl
GRCm381578,947,724 - 79,005,869 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1578,947,724 - 79,005,869 (+)EnsemblGRCm38mm10GRCm38
MGSCv371578,778,154 - 78,836,299 (+)NCBIGRCm37mm9NCBIm37
MGSCv361578,774,979 - 78,833,124 (+)NCBImm8
Celera1581,078,111 - 81,107,504 (+)NCBICelera
Cytogenetic Map15E1NCBI
cM Map1537.7NCBI
Triobp
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.27110,505,916 - 110,569,301 (+)NCBImRatBN7.2
Rnor_6.0 Ensembl7120,176,530 - 120,230,420 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.07120,173,892 - 120,237,145 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.07120,168,221 - 120,228,826 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47116,917,008 - 116,969,695 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.17116,980,831 - 116,993,049 (+)NCBI
Celera7106,842,713 - 106,896,626 (+)NCBICelera
Cytogenetic Map7q34NCBI
TRIOBP
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11026,856,981 - 26,913,330 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1026,857,678 - 26,911,083 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1026,811,904 - 26,834,990 (-)NCBI
ROS_Cfam_1.01027,648,784 - 27,671,889 (-)NCBI
UMICH_Zoey_3.11027,371,705 - 27,394,760 (-)NCBI
UNSW_CanFamBas_1.01027,680,414 - 27,703,444 (-)NCBI
UU_Cfam_GSD_1.01027,857,643 - 27,880,686 (-)NCBI
LOC101970726
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494510,327,377 - 10,380,012 (-)NCBI
SpeTri2.0NW_0049364923,337,791 - 3,390,420 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TRIOBP
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl510,066,086 - 10,126,491 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1510,066,080 - 10,132,668 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.257,561,822 - 7,597,543 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103223289
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11920,447,340 - 20,476,669 (+)NCBI
Vero_WHO_p1.0NW_023666045105,344,581 - 105,372,614 (-)NCBI
Triobp
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462475210,130,857 - 10,186,242 (-)NCBI

Position Markers
SHGC-32573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372238,170,347 - 38,170,497UniSTSGRCh37
Build 362236,500,293 - 36,500,443RGDNCBI36
Celera2221,972,159 - 21,972,309RGD
Cytogenetic Map22q13.1UniSTS
HuRef2221,137,590 - 21,137,740UniSTS
Stanford-G3 RH Map221147.0UniSTS
GeneMap99-GB4 RH Map22123.98UniSTS
Whitehead-RH Map22120.1UniSTS
NCBI RH Map22154.0UniSTS
GeneMap99-G3 RH Map221147.0UniSTS
RH70132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372238,149,039 - 38,149,194UniSTSGRCh37
Build 362236,478,985 - 36,479,140RGDNCBI36
Celera2221,950,845 - 21,951,000RGD
Cytogenetic Map22q13.1UniSTS
HuRef2221,116,205 - 21,116,360UniSTS
GeneMap99-GB4 RH Map22114.21UniSTS
STS-R01098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372238,172,353 - 38,172,521UniSTSGRCh37
Build 362236,502,299 - 36,502,467RGDNCBI36
Celera2221,974,165 - 21,974,333RGD
Cytogenetic Map22q13.1UniSTS
HuRef2221,139,596 - 21,139,764UniSTS
GeneMap99-GB4 RH Map22114.21UniSTS
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
AU048745  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p24.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map14q31.3UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map2q14.2-q14.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic MapXq23UniSTS
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
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
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
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

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:8120
Count of miRNA genes:1338
Interacting mature miRNAs:1778
Transcripts:ENST00000331103, ENST00000344404, ENST00000403663, ENST00000406386, ENST00000407319, ENST00000413051, ENST00000417857, ENST00000418339, ENST00000428075, ENST00000452519, ENST00000492485
Prediction methods:Microtar, Miranda, Rnahybrid
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.


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 2217 2402 1033 173 945 24 3288 1221 799 157 1248 1304 157 1 1204 1983 4
Low 222 589 693 451 1005 441 1069 976 2935 262 212 309 18 805 2 2
Below cutoff 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001039141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_007032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB015343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF281030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL713698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW444985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM682463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ880866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU621193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU675400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX342673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA790674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ228003 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ228004 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ228005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KX533494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z83844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000331103
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,754,882 - 37,755,510 (+)Ensembl
RefSeq Acc Id: ENST00000344404   ⟹   ENSP00000340312
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,697,621 - 37,774,048 (+)Ensembl
RefSeq Acc Id: ENST00000403663   ⟹   ENSP00000386026
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,746,233 - 37,774,140 (+)Ensembl
RefSeq Acc Id: ENST00000407319   ⟹   ENSP00000383913
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,746,238 - 37,760,346 (+)Ensembl
RefSeq Acc Id: ENST00000413051   ⟹   ENSP00000400680
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,746,322 - 37,757,963 (+)Ensembl
RefSeq Acc Id: ENST00000417857   ⟹   ENSP00000387881
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,751,398 - 37,758,047 (+)Ensembl
RefSeq Acc Id: ENST00000418339   ⟹   ENSP00000396946
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,750,997 - 37,757,982 (+)Ensembl
RefSeq Acc Id: ENST00000428075   ⟹   ENSP00000399006
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,746,270 - 37,758,135 (+)Ensembl
RefSeq Acc Id: ENST00000452519   ⟹   ENSP00000407542
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,751,385 - 37,755,574 (+)Ensembl
RefSeq Acc Id: ENST00000492485
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,697,621 - 37,726,570 (+)Ensembl
RefSeq Acc Id: ENST00000644935   ⟹   ENSP00000496394
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,697,048 - 37,776,556 (+)Ensembl
RefSeq Acc Id: NM_001039141   ⟹   NP_001034230
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,697,048 - 37,776,556 (+)NCBI
GRCh372238,092,995 - 38,172,563 (+)ENTREZGENE
Build 362236,423,574 - 36,502,509 (+)NCBI Archive
HuRef2221,059,927 - 21,139,806 (+)ENTREZGENE
CHM1_12238,051,700 - 38,131,297 (+)NCBI
Sequence:
RefSeq Acc Id: NM_007032   ⟹   NP_008963
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,746,234 - 37,776,556 (+)NCBI
GRCh372238,092,995 - 38,172,563 (+)ENTREZGENE
Build 362236,472,187 - 36,502,509 (+)NCBI Archive
HuRef2221,059,927 - 21,139,806 (+)ENTREZGENE
CHM1_12238,100,986 - 38,131,297 (+)NCBI
Sequence:
RefSeq Acc Id: NM_138632   ⟹   NP_619538
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,746,234 - 37,759,954 (+)NCBI
GRCh372238,092,995 - 38,172,563 (+)ENTREZGENE
Build 362236,472,187 - 36,485,907 (+)NCBI Archive
HuRef2221,059,927 - 21,139,806 (+)ENTREZGENE
CHM1_12238,100,986 - 38,114,692 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001034230   ⟸   NM_001039141
- Peptide Label: isoform 6
- UniProtKB: Q9H2D6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_008963   ⟸   NM_007032
- Peptide Label: isoform 1
- UniProtKB: Q9H2D6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_619538   ⟸   NM_138632
- Peptide Label: isoform 2
- UniProtKB: Q9H2D6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000400680   ⟸   ENST00000413051
RefSeq Acc Id: ENSP00000407542   ⟸   ENST00000452519
RefSeq Acc Id: ENSP00000399006   ⟸   ENST00000428075
RefSeq Acc Id: ENSP00000386026   ⟸   ENST00000403663
RefSeq Acc Id: ENSP00000387881   ⟸   ENST00000417857
RefSeq Acc Id: ENSP00000396946   ⟸   ENST00000418339
RefSeq Acc Id: ENSP00000383913   ⟸   ENST00000407319
RefSeq Acc Id: ENSP00000496394   ⟸   ENST00000644935
RefSeq Acc Id: ENSP00000340312   ⟸   ENST00000344404
Protein Domains
PH

Promoters
RGD ID:6799867
Promoter ID:HG_KWN:42732
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:ENST00000396964,   ENST00000406386,   UC003ATR.1,   UC003ATS.1,   UC003ATT.1,   UC003ATU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362236,422,639 - 36,423,139 (+)MPROMDB
RGD ID:6799868
Promoter ID:HG_KWN:42733
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000407319,   NM_007032,   OTTHUMT00000319450
Position:
Human AssemblyChrPosition (strand)Source
Build 362236,471,656 - 36,472,582 (+)MPROMDB
RGD ID:6800436
Promoter ID:HG_KWN:42734
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000319446,   OTTHUMT00000319447,   OTTHUMT00000319448,   OTTHUMT00000319449
Position:
Human AssemblyChrPosition (strand)Source
Build 362236,475,966 - 36,477,467 (+)MPROMDB
RGD ID:13604006
Promoter ID:EPDNEW_H28186
Type:initiation region
Name:TRIOBP_2
Description:TRIO and F-actin binding protein
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28187  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,697,048 - 37,697,108EPDNEW
RGD ID:13604004
Promoter ID:EPDNEW_H28187
Type:initiation region
Name:TRIOBP_1
Description:TRIO and F-actin binding protein
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28186  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,746,263 - 37,746,323EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001039141.3(TRIOBP):c.1039C>T (p.Arg347Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000001555]|not provided [RCV000727382] Chr22:37723595 [GRCh38]
Chr22:38119602 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.1741C>T (p.Gln581Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000001556] Chr22:37724297 [GRCh38]
Chr22:38120304 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.889C>T (p.Gln297Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000001557] Chr22:37723445 [GRCh38]
Chr22:38119452 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.2362C>T (p.Arg788Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000001558] Chr22:37724918 [GRCh38]
Chr22:38120925 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.3202C>T (p.Arg1068Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000001559] Chr22:37725758 [GRCh38]
Chr22:38121765 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.3349C>T (p.Arg1117Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000001560] Chr22:37725905 [GRCh38]
Chr22:38121912 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.3202_3203del (p.Asp1069fs) deletion Deafness, autosomal recessive 28 [RCV000001561] Chr22:37725758..37725759 [GRCh38]
Chr22:38121765..38121766 [GRCh37]
Chr22:22q13.1
pathogenic
TRIOBP, 1-BP INS, 3225C insertion Deafness, autosomal recessive 28 [RCV000001562] Chr22:22q13.1 pathogenic
NM_001039141.3(TRIOBP):c.1446C>A (p.Ala482=) single nucleotide variant not provided [RCV000727904] Chr22:37724002 [GRCh38]
Chr22:38120009 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3892C>T (p.Arg1298Cys) single nucleotide variant not provided [RCV000729470] Chr22:37726448 [GRCh38]
Chr22:38122455 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.2(TRIOBP):c.6325-2708T>C single nucleotide variant Lung cancer [RCV000102060] Chr22:37762962 [GRCh38]
Chr22:38158969 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.-14C>G single nucleotide variant not specified [RCV000036815] Chr22:37701352 [GRCh38]
Chr22:38097359 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.202A>G (p.Thr68Ala) single nucleotide variant not specified [RCV000036816] Chr22:37710514 [GRCh38]
Chr22:38106521 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.391G>A (p.Gly131Ser) single nucleotide variant not provided [RCV000713875]|not specified [RCV000036817] Chr22:37713346 [GRCh38]
Chr22:38109353 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.3975G>A (p.Gln1325=) single nucleotide variant not specified [RCV000036818] Chr22:37733325 [GRCh38]
Chr22:38129332 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.4077T>C (p.Pro1359=) single nucleotide variant not provided [RCV000902443]|not specified [RCV000036819] Chr22:37734413 [GRCh38]
Chr22:38130420 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.4099C>T (p.Arg1367Trp) single nucleotide variant not specified [RCV000036820] Chr22:37734435 [GRCh38]
Chr22:38130442 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4116G>T (p.Glu1372Asp) single nucleotide variant not specified [RCV000036821] Chr22:37734452 [GRCh38]
Chr22:38130459 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.4129T>C (p.Trp1377Arg) single nucleotide variant not specified [RCV000036822] Chr22:37734465 [GRCh38]
Chr22:38130472 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.4178C>T (p.Pro1393Leu) single nucleotide variant not provided [RCV000840103]|not specified [RCV000036823] Chr22:37734514 [GRCh38]
Chr22:38130521 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.4333A>G (p.Arg1445Gly) single nucleotide variant not provided [RCV000963406]|not specified [RCV000036824] Chr22:37734669 [GRCh38]
Chr22:38130676 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.5052G>T (p.Thr1684=) single nucleotide variant not specified [RCV000036825] Chr22:37735388 [GRCh38]
Chr22:38131395 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.5224C>T (p.Leu1742Phe) single nucleotide variant Inborn genetic diseases [RCV000622523]|not provided [RCV000963732]|not specified [RCV000036826] Chr22:37740934 [GRCh38]
Chr22:38136941 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.5487+9A>G single nucleotide variant not provided [RCV000713876]|not specified [RCV000036827] Chr22:37754993 [GRCh38]
Chr22:38151000 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.5488-7del deletion not specified [RCV000036828] Chr22:37755094 [GRCh38]
Chr22:38151101 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.5550G>A (p.Val1850=) single nucleotide variant not specified [RCV000036829] Chr22:37755163 [GRCh38]
Chr22:38151170 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6007G>A (p.Gly2003Ser) single nucleotide variant not specified [RCV000036830] Chr22:37757932 [GRCh38]
Chr22:38153939 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6135C>T (p.Pro2045=) single nucleotide variant not provided [RCV000969750]|not specified [RCV000036831] Chr22:37758060 [GRCh38]
Chr22:38154067 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.6272G>C (p.Ser2091Thr) single nucleotide variant not provided [RCV000923562]|not specified [RCV000036832] Chr22:37759212 [GRCh38]
Chr22:38155219 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6498C>T (p.Tyr2166=) single nucleotide variant not specified [RCV000036833] Chr22:37768099 [GRCh38]
Chr22:38164106 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala) single nucleotide variant not provided [RCV000840104]|not specified [RCV000036834] Chr22:37771699 [GRCh38]
Chr22:38167706 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.6324+226A>G single nucleotide variant not provided [RCV000713874]|not specified [RCV000041122] Chr22:37759490 [GRCh38]
Chr22:38155497 [GRCh37]
Chr22:22q13.1
benign
GRCh38/hg38 22q12.3-13.1(chr22:35333993-38900177)x1 copy number loss See cases [RCV000051364] Chr22:35333993..38900177 [GRCh38]
Chr22:35729986..39296182 [GRCh37]
Chr22:34059986..37626128 [NCBI36]
Chr22:22q12.3-13.1
pathogenic
GRCh38/hg38 22q12.3-13.1(chr22:36859030-39236985)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051366]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051366]|See cases [RCV000051366] Chr22:36859030..39236985 [GRCh38]
Chr22:37255072..39632990 [GRCh37]
Chr22:35585018..37962936 [NCBI36]
Chr22:22q12.3-13.1
pathogenic
GRCh38/hg38 22q13.1(chr22:37721777-38886664)x1 copy number loss See cases [RCV000051367] Chr22:37721777..38886664 [GRCh38]
Chr22:38117784..39282669 [GRCh37]
Chr22:36447730..37612615 [NCBI36]
Chr22:22q13.1
pathogenic
GRCh38/hg38 22q12.3-13.1(chr22:36068124-38002382)x3 copy number gain See cases [RCV000051683] Chr22:36068124..38002382 [GRCh38]
Chr22:36464172..38398389 [GRCh37]
Chr22:34794118..36728335 [NCBI36]
Chr22:22q12.3-13.1
pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3 copy number gain See cases [RCV000051684] Chr22:37061769..50738932 [GRCh38]
Chr22:37457809..51177360 [GRCh37]
Chr22:35787755..49524226 [NCBI36]
Chr22:22q12.3-13.33
pathogenic
GRCh38/hg38 22q13.1-13.2(chr22:37721797-40860953)x3 copy number gain See cases [RCV000051685] Chr22:37721797..40860953 [GRCh38]
Chr22:38117804..41256957 [GRCh37]
Chr22:36447750..39586903 [NCBI36]
Chr22:22q13.1-13.2
pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:33768441-50739977)x3 copy number gain See cases [RCV000051682] Chr22:33768441..50739977 [GRCh38]
Chr22:34164428..51178405 [GRCh37]
Chr22:32494428..49525271 [NCBI36]
Chr22:22q12.3-13.33
pathogenic
NM_001039141.2(TRIOBP):c.382G>A (p.Glu128Lys) single nucleotide variant Malignant melanoma [RCV000072964] Chr22:37713337 [GRCh38]
Chr22:38109344 [GRCh37]
Chr22:36439290 [NCBI36]
Chr22:22q13.1
not provided
NM_001039141.3(TRIOBP):c.1740C>A (p.Ala580=) single nucleotide variant not specified [RCV000179802] Chr22:37724296 [GRCh38]
Chr22:38120303 [GRCh37]
Chr22:36450249 [NCBI36]
Chr22:22q13.1
benign|not provided
NM_001039141.2(TRIOBP):c.2332C>T (p.Pro778Ser) single nucleotide variant Malignant melanoma [RCV000063909] Chr22:37724888 [GRCh38]
Chr22:38120895 [GRCh37]
Chr22:36450841 [NCBI36]
Chr22:22q13.1
not provided
NM_001039141.2(TRIOBP):c.3300C>T (p.Ser1100=) single nucleotide variant Malignant melanoma [RCV000063910] Chr22:37725856 [GRCh38]
Chr22:38121863 [GRCh37]
Chr22:36451809 [NCBI36]
Chr22:22q13.1
not provided
NM_001039141.3(TRIOBP):c.2018G>A (p.Arg673Lys) single nucleotide variant Deafness, autosomal recessive 28 [RCV000660494] Chr22:37724574 [GRCh38]
Chr22:38120581 [GRCh37]
Chr22:22q13.1
uncertain significance
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.3460_3461del (p.Leu1154fs) microsatellite Autosomal recessive nonsyndromic deafness [RCV001291491] Chr22:37726012..37726013 [GRCh38]
Chr22:38122019..38122020 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.815C>A (p.Thr272Lys) single nucleotide variant Deafness, autosomal recessive 28 [RCV000144088]|not provided [RCV000179801] Chr22:37723371 [GRCh38]
Chr22:38119378 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance|not provided
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.1591G>A (p.Ala531Thr) single nucleotide variant not specified [RCV000202789] Chr22:37724147 [GRCh38]
Chr22:38120154 [GRCh37]
Chr22:22q13.1
likely benign
GRCh38/hg38 22q13.1(chr22:37447222-39103680)x1 copy number loss See cases [RCV000141783] Chr22:37447222..39103680 [GRCh38]
Chr22:37843259..39499685 [GRCh37]
Chr22:36173205..37829631 [NCBI36]
Chr22:22q13.1
pathogenic
GRCh38/hg38 22q13.1(chr22:37537317-37803357)x3 copy number gain See cases [RCV000142655] Chr22:37537317..37803357 [GRCh38]
Chr22:37933324..38199364 [GRCh37]
Chr22:36263270..36529310 [NCBI36]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.7017C>T (p.Ile2339=) single nucleotide variant not specified [RCV000156068] Chr22:37772681 [GRCh38]
Chr22:38168688 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4621G>A (p.Ala1541Thr) single nucleotide variant not specified [RCV000156102] Chr22:37734957 [GRCh38]
Chr22:38130964 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4645C>T (p.Arg1549Cys) single nucleotide variant not specified [RCV000156521] Chr22:37734981 [GRCh38]
Chr22:38130988 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4135C>T (p.Pro1379Ser) single nucleotide variant not specified [RCV000156574] Chr22:37734471 [GRCh38]
Chr22:38130478 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6324+191G>A single nucleotide variant not specified [RCV000156666] Chr22:37759455 [GRCh38]
Chr22:38155462 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4244G>A (p.Ser1415Asn) single nucleotide variant not specified [RCV000156672] Chr22:37734580 [GRCh38]
Chr22:38130587 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5588C>T (p.Ala1863Val) single nucleotide variant not provided [RCV000969975]|not specified [RCV000154655] Chr22:37755560 [GRCh38]
Chr22:38151567 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.4101G>A (p.Arg1367=) single nucleotide variant not specified [RCV000156764] Chr22:37734437 [GRCh38]
Chr22:38130444 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4271T>C (p.Leu1424Pro) single nucleotide variant not specified [RCV000156834] Chr22:37734607 [GRCh38]
Chr22:38130614 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.202A>T (p.Thr68Ser) single nucleotide variant not specified [RCV000152129] Chr22:37710514 [GRCh38]
Chr22:38106521 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.265C>G (p.Pro89Ala) single nucleotide variant not provided [RCV000955605]|not specified [RCV000152130] Chr22:37713220 [GRCh38]
Chr22:38109227 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.4009C>G (p.Gln1337Glu) single nucleotide variant not specified [RCV000152132] Chr22:37733359 [GRCh38]
Chr22:38129366 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4329A>G (p.Leu1443=) single nucleotide variant not provided [RCV000838005]|not specified [RCV000152134] Chr22:37734665 [GRCh38]
Chr22:38130672 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4935A>G (p.Ala1645=) single nucleotide variant not provided [RCV000885102]|not specified [RCV000152136] Chr22:37735271 [GRCh38]
Chr22:38131278 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5117A>G (p.Glu1706Gly) single nucleotide variant not specified [RCV000152137] Chr22:37738652 [GRCh38]
Chr22:38134659 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5886A>G (p.Pro1962=) single nucleotide variant not specified [RCV000152140] Chr22:37757811 [GRCh38]
Chr22:38153818 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5693C>T (p.Ser1898Leu) single nucleotide variant not specified [RCV000152141] Chr22:37757618 [GRCh38]
Chr22:38153625 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5936T>C (p.Leu1979Pro) single nucleotide variant not specified [RCV000152142] Chr22:37757861 [GRCh38]
Chr22:38153868 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6184A>G (p.Ser2062Gly) single nucleotide variant not specified [RCV000152143] Chr22:37758109 [GRCh38]
Chr22:38154116 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6324+9G>A single nucleotide variant not specified [RCV000152144] Chr22:37759273 [GRCh38]
Chr22:38155280 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6324+194A>G single nucleotide variant not specified [RCV000152146] Chr22:37759458 [GRCh38]
Chr22:38155465 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6325-10C>T single nucleotide variant not specified [RCV000152147] Chr22:37765660 [GRCh38]
Chr22:38161667 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6362C>T (p.Ser2121Leu) single nucleotide variant Deafness, autosomal recessive 28 [RCV000784920]|not provided [RCV001288530]|not specified [RCV000152148] Chr22:37765707 [GRCh38]
Chr22:38161714 [GRCh37]
Chr22:22q13.1
benign|likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.6455C>T (p.Thr2152Met) single nucleotide variant not specified [RCV000152149] Chr22:37765800 [GRCh38]
Chr22:38161807 [GRCh37]
Chr22:22q13.1
benign|uncertain significance
NM_001039141.3(TRIOBP):c.6472+10C>T single nucleotide variant not provided [RCV000973626]|not specified [RCV000152150] Chr22:37765827 [GRCh38]
Chr22:38161834 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=) single nucleotide variant Deafness, autosomal recessive 28 [RCV001001688]|not provided [RCV000890423]|not specified [RCV000152151] Chr22:37769267 [GRCh38]
Chr22:38165274 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.6598C>T (p.Arg2200Ter) single nucleotide variant Nonsyndromic hearing loss and deafness [RCV000152152] Chr22:37769050 [GRCh38]
Chr22:38165057 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.6936+13G>T single nucleotide variant not specified [RCV000152154] Chr22:37771749 [GRCh38]
Chr22:38167756 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6961T>C (p.Tyr2321His) single nucleotide variant not specified [RCV000152155] Chr22:37772625 [GRCh38]
Chr22:38168632 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.*2+10G>A single nucleotide variant not specified [RCV000152156] Chr22:37772774 [GRCh38]
Chr22:38168781 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.483G>A (p.Glu161=) single nucleotide variant not provided [RCV000724128]|not specified [RCV000155301] Chr22:37715789 [GRCh38]
Chr22:38111796 [GRCh37]
Chr22:22q13.1
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.584C>T (p.Thr195Ile) single nucleotide variant Deafness, autosomal recessive 28 [RCV001286605]|not provided [RCV000843701]|not specified [RCV000155302] Chr22:37715890 [GRCh38]
Chr22:38111897 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.4139A>G (p.Glu1380Gly) single nucleotide variant not specified [RCV000155303] Chr22:37734475 [GRCh38]
Chr22:38130482 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4666G>A (p.Glu1556Lys) single nucleotide variant not provided [RCV001355579]|not specified [RCV000155304] Chr22:37735002 [GRCh38]
Chr22:38131009 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5358G>T (p.Ser1786=) single nucleotide variant not specified [RCV000155305] Chr22:37751807 [GRCh38]
Chr22:38147814 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5544C>T (p.Tyr1848=) single nucleotide variant not specified [RCV000155306] Chr22:37755157 [GRCh38]
Chr22:38151164 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5767G>A (p.Ala1923Thr) single nucleotide variant not provided [RCV001517721]|not specified [RCV000155307] Chr22:37757692 [GRCh38]
Chr22:38153699 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.477G>T (p.Arg159Ser) single nucleotide variant not provided [RCV000830829]|not specified [RCV000152131] Chr22:37715783 [GRCh38]
Chr22:38111790 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4031G>A (p.Arg1344Gln) single nucleotide variant Deafness [RCV000509516]|Deafness, autosomal recessive 28 [RCV000664422]|not provided [RCV000442379]|not specified [RCV000152133] Chr22:37733381 [GRCh38]
Chr22:38129388 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001039141.3(TRIOBP):c.4643C>T (p.Pro1548Leu) single nucleotide variant not provided [RCV000974332]|not specified [RCV000152135] Chr22:37734979 [GRCh38]
Chr22:38130986 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.5166C>G (p.Asp1722Glu) single nucleotide variant not specified [RCV000152138] Chr22:37738701 [GRCh38]
Chr22:38134708 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5349A>T (p.Gly1783=) single nucleotide variant not specified [RCV000152139] Chr22:37751798 [GRCh38]
Chr22:38147805 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6324+162G>A single nucleotide variant not specified [RCV000152145] Chr22:37759426 [GRCh38]
Chr22:38155433 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.6736G>A (p.Glu2246Lys) single nucleotide variant not provided [RCV000973056]|not specified [RCV000152153] Chr22:37769262 [GRCh38]
Chr22:38165269 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.6803G>A (p.Gly2268Asp) single nucleotide variant Hearing impairment [RCV001375240]|not specified [RCV000155715] Chr22:37769329 [GRCh38]
Chr22:38165336 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3068C>T (p.Ala1023Val) single nucleotide variant not provided [RCV000179803] Chr22:37725624 [GRCh38]
Chr22:38121631 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1193_1195del (p.Gln398del) deletion Deafness, autosomal recessive 28 [RCV000990437]|not specified [RCV000179804] Chr22:37723748..37723750 [GRCh38]
Chr22:38119755..38119757 [GRCh37]
Chr22:22q13.1
benign
GRCh37/hg19 22q12.3-13.1(chr22:37090025-39601950)x3 copy number gain See cases [RCV000446037] Chr22:37090025..39601950 [GRCh37]
Chr22:22q12.3-13.1
uncertain significance
GRCh37/hg19 22q12.3-13.1(chr22:35680095-38098981)x1 copy number loss See cases [RCV000207444] Chr22:35680095..38098981 [GRCh37]
Chr22:22q12.3-13.1
pathogenic
NM_001039141.3(TRIOBP):c.4497T>G (p.Thr1499=) single nucleotide variant not specified [RCV000223500] Chr22:37734833 [GRCh38]
Chr22:38130840 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6771G>A (p.Gln2257=) single nucleotide variant not provided [RCV000731421]|not specified [RCV000215313] Chr22:37769297 [GRCh38]
Chr22:38165304 [GRCh37]
Chr22:22q13.1
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.5575C>G (p.His1859Asp) single nucleotide variant not specified [RCV000215350] Chr22:37755188 [GRCh38]
Chr22:38151195 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5705A>C (p.Lys1902Thr) single nucleotide variant Deafness, autosomal recessive 28 [RCV000765639]|not provided [RCV000727151]|not specified [RCV000219620] Chr22:37757630 [GRCh38]
Chr22:38153637 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5266C>T (p.Arg1756Trp) single nucleotide variant not specified [RCV000221922] Chr22:37740976 [GRCh38]
Chr22:38136983 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6806A>G (p.Asn2269Ser) single nucleotide variant not provided [RCV000905231]|not specified [RCV000221957] Chr22:37769332 [GRCh38]
Chr22:38165339 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.5782A>G (p.Ile1928Val) single nucleotide variant not specified [RCV000222013] Chr22:37757707 [GRCh38]
Chr22:38153714 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4773C>T (p.Ala1591=) single nucleotide variant not specified [RCV000213125] Chr22:37735109 [GRCh38]
Chr22:38131116 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6556G>A (p.Gly2186Ser) single nucleotide variant not provided [RCV000827584]|not specified [RCV000217336] Chr22:37768157 [GRCh38]
Chr22:38164164 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.3948G>A (p.Arg1316=) single nucleotide variant not specified [RCV000213230] Chr22:37733298 [GRCh38]
Chr22:38129305 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5528C>T (p.Thr1843Met) single nucleotide variant not specified [RCV000217372] Chr22:37755141 [GRCh38]
Chr22:38151148 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6575+14G>A single nucleotide variant not specified [RCV000222232] Chr22:37768190 [GRCh38]
Chr22:38164197 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4165C>A (p.Leu1389Ile) single nucleotide variant not provided [RCV000905229]|not specified [RCV000222264] Chr22:37734501 [GRCh38]
Chr22:38130508 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.5393C>T (p.Ser1798Leu) single nucleotide variant not specified [RCV000213426] Chr22:37754890 [GRCh38]
Chr22:38150897 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5167C>A (p.Gln1723Lys) single nucleotide variant not specified [RCV000217627] Chr22:37738702 [GRCh38]
Chr22:38134709 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6571C>T (p.His2191Tyr) single nucleotide variant not provided [RCV000905230]|not specified [RCV000217679] Chr22:37768172 [GRCh38]
Chr22:38164179 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.4572G>A (p.Glu1524=) single nucleotide variant not specified [RCV000220150] Chr22:37734908 [GRCh38]
Chr22:38130915 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.3652A>G (p.Ile1218Val) single nucleotide variant not provided [RCV000519606] Chr22:37726208 [GRCh38]
Chr22:38122215 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6039C>G (p.Pro2013=) single nucleotide variant not specified [RCV000213655] Chr22:37757964 [GRCh38]
Chr22:38153971 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5378A>C (p.Glu1793Ala) single nucleotide variant not provided [RCV000893082]|not specified [RCV000220382] Chr22:37751827 [GRCh38]
Chr22:38147834 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4062+5G>A single nucleotide variant not specified [RCV000220498] Chr22:37733417 [GRCh38]
Chr22:38129424 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.7032G>A (p.Glu2344=) single nucleotide variant not provided [RCV000905232]|not specified [RCV000215732] Chr22:37772696 [GRCh38]
Chr22:38168703 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.4703C>G (p.Ala1568Gly) single nucleotide variant not provided [RCV000926485]|not specified [RCV000214164] Chr22:37735039 [GRCh38]
Chr22:38131046 [GRCh37]
Chr22:22q13.1
benign|uncertain significance
NM_001039141.3(TRIOBP):c.6515G>A (p.Arg2172Gln) single nucleotide variant Deafness, autosomal recessive 28 [RCV000765640]|not specified [RCV000215900] Chr22:37768116 [GRCh38]
Chr22:38164123 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.5488-14C>T single nucleotide variant not specified [RCV000218344] Chr22:37755087 [GRCh38]
Chr22:38151094 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.111C>G (p.Tyr37Ter) single nucleotide variant not specified [RCV000220716] Chr22:37701476 [GRCh38]
Chr22:38097483 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5519G>A (p.Arg1840His) single nucleotide variant not specified [RCV000214241] Chr22:37755132 [GRCh38]
Chr22:38151139 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.409A>G (p.Ser137Gly) single nucleotide variant not specified [RCV000218540] Chr22:37713364 [GRCh38]
Chr22:38109371 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.-3A>G single nucleotide variant not specified [RCV000216202] Chr22:37701363 [GRCh38]
Chr22:38097370 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.273A>G (p.Ala91=) single nucleotide variant not specified [RCV000216265] Chr22:37713228 [GRCh38]
Chr22:38109235 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6170G>A (p.Arg2057His) single nucleotide variant not specified [RCV000221099] Chr22:37758095 [GRCh38]
Chr22:38154102 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.504C>A (p.Asp168Glu) single nucleotide variant not provided [RCV000881690]|not specified [RCV000214626] Chr22:37715810 [GRCh38]
Chr22:38111817 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.96C>T (p.Ala32=) single nucleotide variant not specified [RCV000221229] Chr22:37701461 [GRCh38]
Chr22:38097468 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6196G>A (p.Glu2066Lys) single nucleotide variant not specified [RCV000214780] Chr22:37758121 [GRCh38]
Chr22:38154128 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4548T>C (p.Pro1516=) single nucleotide variant not specified [RCV000216495] Chr22:37734884 [GRCh38]
Chr22:38130891 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6986G>A (p.Ser2329Asn) single nucleotide variant not specified [RCV000218912] Chr22:37772650 [GRCh38]
Chr22:38168657 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6205G>A (p.Glu2069Lys) single nucleotide variant not specified [RCV000219084] Chr22:37758130 [GRCh38]
Chr22:38154137 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4783C>T (p.Arg1595Cys) single nucleotide variant not provided [RCV000731187]|not specified [RCV000216779] Chr22:37735119 [GRCh38]
Chr22:38131126 [GRCh37]
Chr22:22q13.1
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.5891G>A (p.Arg1964His) single nucleotide variant not specified [RCV000221663] Chr22:37757816 [GRCh38]
Chr22:38153823 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6324+240G>A single nucleotide variant not specified [RCV000223340] Chr22:37759504 [GRCh38]
Chr22:38155511 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.2869C>G (p.Gln957Glu) single nucleotide variant not provided [RCV000756806] Chr22:37725425 [GRCh38]
Chr22:38121432 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3386C>T (p.Ala1129Val) single nucleotide variant not provided [RCV000756807] Chr22:37725942 [GRCh38]
Chr22:38121949 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.7044T>C (p.Leu2348=) single nucleotide variant not provided [RCV000756808] Chr22:37772708 [GRCh38]
Chr22:38168715 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.2582G>A (p.Arg861Gln) single nucleotide variant not specified [RCV000238865] Chr22:37725138 [GRCh38]
Chr22:38121145 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3232C>T (p.Arg1078Cys) single nucleotide variant not specified [RCV000239147] Chr22:37725788 [GRCh38]
Chr22:38121795 [GRCh37]
Chr22:22q13.1
benign|likely benign|conflicting interpretations of pathogenicity
NM_001039141.3(TRIOBP):c.2064C>A (p.Ser688Arg) single nucleotide variant Deafness, autosomal recessive 28 [RCV000626273] Chr22:37724620 [GRCh38]
Chr22:38120627 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4103G>A (p.Arg1368Gln) single nucleotide variant not specified [RCV000600658] Chr22:37734439 [GRCh38]
Chr22:38130446 [GRCh37]
Chr22:22q13.1
likely benign
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 copy number gain See cases [RCV000240091] Chr22:16054691..51237518 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.4419G>A (p.Pro1473=) single nucleotide variant not specified [RCV000248574] Chr22:37734755 [GRCh38]
Chr22:38130762 [GRCh37]
Chr22:22q13.1
likely benign
GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3 copy number gain See cases [RCV000240469] Chr22:35728929..51220961 [GRCh37]
Chr22:22q12.3-13.33
pathogenic
NM_001039141.3(TRIOBP):c.6472+15_6472+16insC insertion not specified [RCV000249508] Chr22:37765832..37765833 [GRCh38]
Chr22:38161839..38161840 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6472+19dup duplication not specified [RCV000254498] Chr22:37765828..37765829 [GRCh38]
Chr22:38161835..38161836 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6472+14G>T single nucleotide variant not provided [RCV000726072]|not specified [RCV000244968] Chr22:37765831 [GRCh38]
Chr22:38161838 [GRCh37]
Chr22:22q13.1
benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.5764C>T (p.Arg1922Trp) single nucleotide variant not provided [RCV000927547]|not specified [RCV000252969] Chr22:37757689 [GRCh38]
Chr22:38153696 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.3854_3855del (p.Arg1285fs) microsatellite not provided [RCV000267345] Chr22:37726407..37726408 [GRCh38]
Chr22:38122414..38122415 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.3885C>T (p.Ser1295=) single nucleotide variant not specified [RCV000270958] Chr22:37726441 [GRCh38]
Chr22:38122448 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.446C>T (p.Ser149Leu) single nucleotide variant not provided [RCV000371778] Chr22:37713401 [GRCh38]
Chr22:38109408 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5853G>A (p.Leu1951=) single nucleotide variant not provided [RCV000373888]|not specified [RCV001195467] Chr22:37757778 [GRCh38]
Chr22:38153785 [GRCh37]
Chr22:22q13.1
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.2149C>G (p.Gln717Glu) single nucleotide variant Deafness, autosomal recessive 28 [RCV000765638]|not provided [RCV000725895] Chr22:37724705 [GRCh38]
Chr22:38120712 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.634G>A (p.Gly212Ser) single nucleotide variant Deafness, autosomal recessive 28 [RCV001287744]|not provided [RCV000316782] Chr22:37723190 [GRCh38]
Chr22:38119197 [GRCh37]
Chr22:22q13.1
benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.2811C>T (p.Ile937=) single nucleotide variant not provided [RCV000350127] Chr22:37725367 [GRCh38]
Chr22:38121374 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6472+13_6472+14insT insertion not specified [RCV000285971] Chr22:37765830..37765831 [GRCh38]
Chr22:38161837..38161838 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.1874G>C (p.Arg625Thr) single nucleotide variant not provided [RCV000391829] Chr22:37724430 [GRCh38]
Chr22:38120437 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3944G>A (p.Arg1315His) single nucleotide variant not provided [RCV000288899] Chr22:37726500 [GRCh38]
Chr22:38122507 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6472+16G>C single nucleotide variant not provided [RCV000321325] Chr22:37765833 [GRCh38]
Chr22:38161840 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1283C>G (p.Pro428Arg) single nucleotide variant Deafness, autosomal recessive 28 [RCV000765637]|not provided [RCV000393692] Chr22:37723839 [GRCh38]
Chr22:38119846 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3429C>T (p.Ser1143=) single nucleotide variant not provided [RCV000323188] Chr22:37725985 [GRCh38]
Chr22:38121992 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6472+19_6472+20insA insertion not provided [RCV000359137] Chr22:37765836..37765837 [GRCh38]
Chr22:38161843..38161844 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3309C>T (p.His1103=) single nucleotide variant not provided [RCV000360902] Chr22:37725865 [GRCh38]
Chr22:38121872 [GRCh37]
Chr22:22q13.1
conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.3774C>T (p.Pro1258=) single nucleotide variant not provided [RCV000397770] Chr22:37726330 [GRCh38]
Chr22:38122337 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3074G>A (p.Arg1025Gln) single nucleotide variant not specified [RCV000295712] Chr22:37725630 [GRCh38]
Chr22:38121637 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.3899A>G (p.His1300Arg) single nucleotide variant not specified [RCV000328335] Chr22:37726455 [GRCh38]
Chr22:38122462 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.2590C>T (p.Pro864Ser) single nucleotide variant not provided [RCV000364258] Chr22:37725146 [GRCh38]
Chr22:38121153 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6723G>C (p.Leu2241=) single nucleotide variant not provided [RCV000366851] Chr22:37769175 [GRCh38]
Chr22:38165182 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.2201C>T (p.Ser734Phe) single nucleotide variant Deafness, autosomal recessive 28 [RCV001001791]|not provided [RCV000334250] Chr22:37724757 [GRCh38]
Chr22:38120764 [GRCh37]
Chr22:22q13.1
benign|uncertain significance
NM_001039141.3(TRIOBP):c.3084G>A (p.Ser1028=) single nucleotide variant not provided [RCV000369052] Chr22:37725640 [GRCh38]
Chr22:38121647 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6860G>A (p.Arg2287His) single nucleotide variant Deafness, autosomal recessive 28 [RCV000490368] Chr22:37771660 [GRCh38]
Chr22:38167667 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4484A>T (p.Glu1495Val) single nucleotide variant not provided [RCV000833260]|not specified [RCV000606623] Chr22:37734820 [GRCh38]
Chr22:38130827 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6360C>T (p.Ser2120=) single nucleotide variant not provided [RCV000596783] Chr22:37765705 [GRCh38]
Chr22:38161712 [GRCh37]
Chr22:22q13.1
conflicting interpretations of pathogenicity|uncertain significance
NM_001039141.3(TRIOBP):c.6324+235C>T single nucleotide variant not specified [RCV000603692] Chr22:37759499 [GRCh38]
Chr22:38155506 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5529G>A (p.Thr1843=) single nucleotide variant not specified [RCV000599724] Chr22:37755142 [GRCh38]
Chr22:38151149 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.650G>A (p.Ser217Asn) single nucleotide variant not specified [RCV000606900] Chr22:37723206 [GRCh38]
Chr22:38119213 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.6123T>A (p.Asn2041Lys) single nucleotide variant not provided [RCV000730493] Chr22:37758048 [GRCh38]
Chr22:38154055 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1263T>C (p.Asn421=) single nucleotide variant not specified [RCV000730494] Chr22:37723819 [GRCh38]
Chr22:38119826 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6818G>A (p.Arg2273His) single nucleotide variant not provided [RCV000523295] Chr22:37769344 [GRCh38]
Chr22:38165351 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.251_254+22del deletion not provided [RCV000597685] Chr22:37710553..37710578 [GRCh38]
Chr22:38106560..38106585 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.4130G>A (p.Trp1377Ter) single nucleotide variant not provided [RCV000599292] Chr22:37734466 [GRCh38]
Chr22:38130473 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.7066_7068del (p.Lys2356del) deletion not provided [RCV000598403] Chr22:37772728..37772730 [GRCh38]
Chr22:38168735..38168737 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1195C>T (p.Arg399Ter) single nucleotide variant not provided [RCV000523834] Chr22:37723751 [GRCh38]
Chr22:38119758 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.6776G>A (p.Arg2259His) single nucleotide variant not specified [RCV000603803] Chr22:37769302 [GRCh38]
Chr22:38165309 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5655C>T (p.Thr1885=) single nucleotide variant not provided [RCV000735069] Chr22:37755627 [GRCh38]
Chr22:38151634 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1225C>T (p.Arg409Trp) single nucleotide variant not specified [RCV000732124] Chr22:37723781 [GRCh38]
Chr22:38119788 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4728T>C (p.Arg1576=) single nucleotide variant not provided [RCV000901476]|not specified [RCV000730233] Chr22:37735064 [GRCh38]
Chr22:38131071 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.3487_3533del (p.Pro1163fs) deletion not provided [RCV000734826] Chr22:37726033..37726079 [GRCh38]
Chr22:38122040..38122086 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.2105A>G (p.Gln702Arg) single nucleotide variant not specified [RCV000732730] Chr22:37724661 [GRCh38]
Chr22:38120668 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.1158C>T (p.Asp386=) single nucleotide variant not specified [RCV000728068] Chr22:37723714 [GRCh38]
Chr22:38119721 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.1213T>C (p.Ser405Pro) single nucleotide variant not provided [RCV000728077] Chr22:37723769 [GRCh38]
Chr22:38119776 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3055G>A (p.Gly1019Arg) single nucleotide variant Deafness, autosomal recessive 28 [RCV000454135] Chr22:37725611 [GRCh38]
Chr22:38121618 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.1447C>T (p.Gln483Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000454233] Chr22:37724003 [GRCh38]
Chr22:38120010 [GRCh37]
Chr22:22q13.1
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 copy number gain See cases [RCV000446956] Chr22:16054691..51220902 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.4062+2T>C single nucleotide variant not provided [RCV000422575] Chr22:37733414 [GRCh38]
Chr22:38129421 [GRCh37]
Chr22:22q13.1
likely pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 copy number gain See cases [RCV000448847] Chr22:16054691..51237463 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.5488-2A>G single nucleotide variant not provided [RCV000480502] Chr22:37755099 [GRCh38]
Chr22:38151106 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.3775G>A (p.Gly1259Arg) single nucleotide variant not provided [RCV000498383] Chr22:37726331 [GRCh38]
Chr22:38122338 [GRCh37]
Chr22:22q13.1
uncertain significance
GRCh37/hg19 22q13.1(chr22:37866631-39054815)x1 copy number loss See cases [RCV000511673] Chr22:37866631..39054815 [GRCh37]
Chr22:22q13.1
pathogenic
GRCh37/hg19 22q12.3-13.1(chr22:36877226-38548989)x1 copy number loss See cases [RCV000512008] Chr22:36877226..38548989 [GRCh37]
Chr22:22q12.3-13.1
pathogenic
NM_001039141.3(TRIOBP):c.6562C>T (p.Arg2188Trp) single nucleotide variant not provided [RCV000493308] Chr22:37768163 [GRCh38]
Chr22:38164170 [GRCh37]
Chr22:22q13.1
uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) copy number gain See cases [RCV000510873] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.5058C>G (p.Pro1686=) single nucleotide variant not provided [RCV000923956]|not specified [RCV000607045] Chr22:37735394 [GRCh38]
Chr22:38131401 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.5247A>G (p.Ser1749=) single nucleotide variant not specified [RCV000602261] Chr22:37740957 [GRCh38]
Chr22:38136964 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.64C>T (p.Arg22Cys) single nucleotide variant not specified [RCV000612125] Chr22:37701429 [GRCh38]
Chr22:38097436 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6324+236G>A single nucleotide variant not specified [RCV000609692] Chr22:37759500 [GRCh38]
Chr22:38155507 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.1306G>A (p.Asp436Asn) single nucleotide variant not specified [RCV000612633] Chr22:37723862 [GRCh38]
Chr22:38119869 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.115-12A>T single nucleotide variant not specified [RCV000615389] Chr22:37710415 [GRCh38]
Chr22:38106422 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5380-14C>T single nucleotide variant not specified [RCV000612987] Chr22:37754863 [GRCh38]
Chr22:38150870 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4726C>T (p.Arg1576Cys) single nucleotide variant not provided [RCV000923126]|not specified [RCV000607520] Chr22:37735062 [GRCh38]
Chr22:38131069 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.118C>T (p.Leu40Phe) single nucleotide variant not provided [RCV000597650] Chr22:37710430 [GRCh38]
Chr22:38106437 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.2589C>A (p.Asn863Lys) single nucleotide variant not specified [RCV000610701] Chr22:37725145 [GRCh38]
Chr22:38121152 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.3145_3146del (p.Glu1048_Ser1049insTer) microsatellite Deafness, autosomal recessive 28 [RCV000585645] Chr22:37725698..37725699 [GRCh38]
Chr22:38121705..38121706 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.5373T>C (p.Pro1791=) single nucleotide variant not specified [RCV000600842] Chr22:37751822 [GRCh38]
Chr22:38147829 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.3954C>T (p.Ser1318=) single nucleotide variant not provided [RCV000904392]|not specified [RCV000608392] Chr22:37733304 [GRCh38]
Chr22:38129311 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.5185-12C>G single nucleotide variant not specified [RCV000611291] Chr22:37740883 [GRCh38]
Chr22:38136890 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3559T>C (p.Phe1187Leu) single nucleotide variant not specified [RCV000614567] Chr22:37726115 [GRCh38]
Chr22:38122122 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.4932C>T (p.Pro1644=) single nucleotide variant not specified [RCV000614707] Chr22:37735268 [GRCh38]
Chr22:38131275 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.1478G>A (p.Ser493Asn) single nucleotide variant Deafness, autosomal recessive 28 [RCV000605383]|not provided [RCV000948135]|not specified [RCV000609850] Chr22:37724034 [GRCh38]
Chr22:38120041 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.7010G>A (p.Arg2337Gln) single nucleotide variant not provided [RCV001358179]|not specified [RCV000604907] Chr22:37772674 [GRCh38]
Chr22:38168681 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.5869C>T (p.Gln1957Ter) single nucleotide variant not specified [RCV000602159] Chr22:37757794 [GRCh38]
Chr22:38153801 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5322+5264G>T single nucleotide variant not specified [RCV000600259] Chr22:37746296 [GRCh38]
Chr22:38142303 [GRCh37]
Chr22:22q13.1
likely benign
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 copy number gain See cases [RCV000512333] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q12.3-13.1(chr22:35674826-39466442)x3 copy number gain See cases [RCV000512385] Chr22:35674826..39466442 [GRCh37]
Chr22:22q12.3-13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.3219G>A (p.Ala1073=) single nucleotide variant not provided [RCV000596656] Chr22:37725775 [GRCh38]
Chr22:38121782 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6957A>G (p.Gly2319=) single nucleotide variant not provided [RCV000597111] Chr22:37772621 [GRCh38]
Chr22:38168628 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV001329528]|Hearing impairment [RCV001375312]|not provided [RCV000760513]|not specified [RCV000601096] Chr22:37735350 [GRCh38]
Chr22:38131357 [GRCh37]
Chr22:22q13.1
pathogenic|likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.4933G>A (p.Ala1645Thr) single nucleotide variant Inborn genetic diseases [RCV000623554] Chr22:37735269 [GRCh38]
Chr22:38131276 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3634_3646del (p.Leu1212fs) deletion Autosomal recessive nonsyndromic deafness [RCV001291492]|Deafness, autosomal recessive 28 [RCV000681528] Chr22:37726189..37726201 [GRCh38]
Chr22:38122196..38122208 [GRCh37]
Chr22:22q13.1
pathogenic|likely pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 copy number gain not provided [RCV000741689] Chr22:16054667..51243435 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 copy number gain not provided [RCV000741691] Chr22:16114244..51195728 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q13.1(chr22:38153637-38165339)x1 copy number loss not provided [RCV000741959] Chr22:38153637..38165339 [GRCh37]
Chr22:22q13.1
benign
GRCh37/hg19 22q13.1(chr22:38153699-38165339)x1 copy number loss not provided [RCV000741960] Chr22:38153699..38165339 [GRCh37]
Chr22:22q13.1
benign
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 copy number gain not provided [RCV000741692] Chr22:16114244..51211392 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.4203G>A (p.Arg1401=) single nucleotide variant not provided [RCV000977317] Chr22:37734539 [GRCh38]
Chr22:38130546 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.1933C>T (p.Gln645Ter) single nucleotide variant not provided [RCV000760498] Chr22:37724489 [GRCh38]
Chr22:38120496 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.2968C>T (p.Arg990Ter) single nucleotide variant not provided [RCV000760557] Chr22:37725524 [GRCh38]
Chr22:38121531 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.6141T>G (p.Thr2047=) single nucleotide variant not provided [RCV000925706] Chr22:37758066 [GRCh38]
Chr22:38154073 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5394G>A (p.Ser1798=) single nucleotide variant not provided [RCV000879942] Chr22:37754891 [GRCh38]
Chr22:38150898 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4953G>A (p.Pro1651=) single nucleotide variant not provided [RCV000937238] Chr22:37735289 [GRCh38]
Chr22:38131296 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4510A>G (p.Arg1504Gly) single nucleotide variant not provided [RCV000906887] Chr22:37734846 [GRCh38]
Chr22:38130853 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.3524C>A (p.Ser1175Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000770881] Chr22:37726080 [GRCh38]
Chr22:38122087 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.131C>G (p.Ser44Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000770882] Chr22:37710443 [GRCh38]
Chr22:38106450 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.6324+233C>G single nucleotide variant not specified [RCV000825255] Chr22:37759497 [GRCh38]
Chr22:38155504 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6324+214G>A single nucleotide variant not specified [RCV000826061] Chr22:37759478 [GRCh38]
Chr22:38155485 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6775C>T (p.Arg2259Cys) single nucleotide variant not specified [RCV000826063] Chr22:37769301 [GRCh38]
Chr22:38165308 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6548G>A (p.Gly2183Asp) single nucleotide variant Deafness, autosomal recessive 28 [RCV000768434] Chr22:37768149 [GRCh38]
Chr22:38164156 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5511C>T (p.Ile1837=) single nucleotide variant not provided [RCV000980956] Chr22:37755124 [GRCh38]
Chr22:38151131 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.154G>A (p.Asp52Asn) single nucleotide variant Deafness, autosomal recessive 28 [RCV000768433] Chr22:37710466 [GRCh38]
Chr22:38106473 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4291G>T (p.Glu1431Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV000770880] Chr22:37734627 [GRCh38]
Chr22:38130634 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.826C>T (p.Pro276Ser) single nucleotide variant Deafness, autosomal recessive 28 [RCV000770883] Chr22:37723382 [GRCh38]
Chr22:38119389 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.4023A>G (p.Gln1341=) single nucleotide variant not provided [RCV000841205] Chr22:37733373 [GRCh38]
Chr22:38129380 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.363C>A (p.Ser121=) single nucleotide variant not provided [RCV000906640]|not specified [RCV000825252] Chr22:37713318 [GRCh38]
Chr22:38109325 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.6324+177G>A single nucleotide variant not specified [RCV000825253] Chr22:37759441 [GRCh38]
Chr22:38155448 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6414G>A (p.Gln2138=) single nucleotide variant not provided [RCV000840085] Chr22:37765759 [GRCh38]
Chr22:38161766 [GRCh37]
Chr22:22q13.1
benign|likely benign
NM_001039141.3(TRIOBP):c.2456T>C (p.Ile819Thr) single nucleotide variant not provided [RCV000842689] Chr22:37725012 [GRCh38]
Chr22:38121019 [GRCh37]
Chr22:22q13.1
likely benign
NC_000022.11:g.(?_37738534)_(37741122_?)del deletion not specified [RCV000826065] Chr22:38134541..38137129 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6792G>A (p.Ser2264=) single nucleotide variant not provided [RCV000914188]|not specified [RCV000825254] Chr22:37769318 [GRCh38]
Chr22:38165325 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6283T>C (p.Ser2095Pro) single nucleotide variant not specified [RCV000825258] Chr22:37759223 [GRCh38]
Chr22:38155230 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.2061_2132del (p.Ser688_Pro711del) deletion Deafness, autosomal recessive 28 [RCV000790953] Chr22:37724598..37724669 [GRCh38]
Chr22:38120605..38120676 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6472+33G>A single nucleotide variant not provided [RCV000844335] Chr22:37765850 [GRCh38]
Chr22:38161857 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6575+96del deletion not provided [RCV000844336] Chr22:37768272 [GRCh38]
Chr22:38164279 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4792C>G (p.Pro1598Ala) single nucleotide variant Deafness, autosomal recessive 28 [RCV001285606]|not provided [RCV000916017] Chr22:37735128 [GRCh38]
Chr22:38131135 [GRCh37]
Chr22:22q13.1
likely benign|uncertain significance
NM_001039141.3(TRIOBP):c.6513C>T (p.Ser2171=) single nucleotide variant not provided [RCV000827580] Chr22:37768114 [GRCh38]
Chr22:38164121 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.1979C>T (p.Ala660Val) single nucleotide variant not provided [RCV000840923] Chr22:37724535 [GRCh38]
Chr22:38120542 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.567G>T (p.Arg189Ser) single nucleotide variant not provided [RCV000993353] Chr22:37715873 [GRCh38]
Chr22:38111880 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6830G>A (p.Arg2277Gln) single nucleotide variant not specified [RCV000826062] Chr22:37769356 [GRCh38]
Chr22:38165363 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6975T>C (p.Tyr2325=) single nucleotide variant not specified [RCV000825257] Chr22:37772639 [GRCh38]
Chr22:38168646 [GRCh37]
Chr22:22q13.1
likely benign
GRCh37/hg19 22q13.1(chr22:38118220-38187935)x3 copy number gain not provided [RCV000846006] Chr22:38118220..38187935 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5949C>T (p.Ser1983=) single nucleotide variant not specified [RCV000825256] Chr22:37757874 [GRCh38]
Chr22:38153881 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6308C>T (p.Pro2103Leu) single nucleotide variant not specified [RCV000826064] Chr22:37759248 [GRCh38]
Chr22:38155255 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.536G>C (p.Arg179Pro) single nucleotide variant Deafness, autosomal recessive 28 [RCV001027970] Chr22:37715842 [GRCh38]
Chr22:38111849 [GRCh37]
Chr22:22q13.1
uncertain significance
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3 copy number gain not provided [RCV001007181] Chr22:30654764..51197838 [GRCh37]
Chr22:22q12.2-13.33
pathogenic
NM_001039141.3(TRIOBP):c.4298C>T (p.Pro1433Leu) single nucleotide variant not provided [RCV000993352] Chr22:37734634 [GRCh38]
Chr22:38130641 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4232_4233del (p.Arg1411fs) microsatellite not provided [RCV001008955] Chr22:37734565..37734566 [GRCh38]
Chr22:38130572..38130573 [GRCh37]
Chr22:22q13.1
likely pathogenic
GRCh37/hg19 22q13.1(chr22:38002218-38973070)x1 copy number loss not provided [RCV001007501] Chr22:38002218..38973070 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.301G>A (p.Ala101Thr) single nucleotide variant not specified [RCV001195469] Chr22:37713256 [GRCh38]
Chr22:38109263 [GRCh37]
Chr22:22q13.1
likely benign
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 copy number gain not provided [RCV000846344] Chr22:16888899..51197838 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.365T>C (p.Leu122Ser) single nucleotide variant not provided [RCV000973625] Chr22:37713320 [GRCh38]
Chr22:38109327 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.3073C>T (p.Arg1025Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV001196643] Chr22:37725629 [GRCh38]
Chr22:38121636 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.6022C>T (p.Arg2008Trp) single nucleotide variant not provided [RCV000993354] Chr22:37757947 [GRCh38]
Chr22:38153954 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4526_4527del (p.Arg1509fs) microsatellite not provided [RCV001009068] Chr22:37734859..37734860 [GRCh38]
Chr22:38130866..38130867 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.5198C>T (p.Pro1733Leu) single nucleotide variant not specified [RCV001195638] Chr22:37740908 [GRCh38]
Chr22:38136915 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.2477C>T (p.Ser826Leu) single nucleotide variant Deafness, autosomal recessive 28 [RCV001001615] Chr22:37725033 [GRCh38]
Chr22:38121040 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.3089C>G (p.Pro1030Arg) single nucleotide variant Deafness, autosomal recessive 28 [RCV001001702] Chr22:37725645 [GRCh38]
Chr22:38121652 [GRCh37]
Chr22:22q13.1
benign
NM_001039141.3(TRIOBP):c.5890C>G (p.Arg1964Gly) single nucleotide variant not specified [RCV001195639] Chr22:37757815 [GRCh38]
Chr22:38153822 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5358G>A (p.Ser1786=) single nucleotide variant not specified [RCV001195468] Chr22:37751807 [GRCh38]
Chr22:38147814 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.4429T>C (p.Trp1477Arg) single nucleotide variant not specified [RCV001195470] Chr22:37734765 [GRCh38]
Chr22:38130772 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.5929C>T (p.Arg1977Trp) single nucleotide variant not specified [RCV001195634] Chr22:37757854 [GRCh38]
Chr22:38153861 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.5193G>C (p.Lys1731Asn) single nucleotide variant not specified [RCV001195637] Chr22:37740903 [GRCh38]
Chr22:38136910 [GRCh37]
Chr22:22q13.1
uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 copy number gain See cases [RCV001263056] Chr22:16197005..51224252 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser) single nucleotide variant Deafness, autosomal recessive 28 [RCV001337110] Chr22:37723520 [GRCh38]
Chr22:38119527 [GRCh37]
Chr22:22q13.1
uncertain significance
GRCh37/hg19 22q13.1(chr22:38155164-38541997) copy number loss Waardenburg syndrome type 2E [RCV001290182] Chr22:38155164..38541997 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.1567C>T (p.Arg523Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV001293894] Chr22:37724123 [GRCh38]
Chr22:38120130 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.3692G>A (p.Arg1231His) single nucleotide variant Hearing impairment [RCV001375314] Chr22:37726248 [GRCh38]
Chr22:38122255 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4436del (p.Gly1479fs) deletion Hearing impairment [RCV001375213] Chr22:37734766 [GRCh38]
Chr22:38130773 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.3232dup (p.Arg1078fs) duplication Deafness, autosomal recessive 28 [RCV001337107] Chr22:37725781..37725782 [GRCh38]
Chr22:38121788..38121789 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.709C>T (p.Arg237Trp) single nucleotide variant not provided [RCV001357186] Chr22:37723265 [GRCh38]
Chr22:38119272 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6328G>A (p.Ala2110Thr) single nucleotide variant Hearing impairment [RCV001375063] Chr22:37765673 [GRCh38]
Chr22:38161680 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1866_1867del (p.Asp622fs) deletion not provided [RCV001356098] Chr22:37724421..37724422 [GRCh38]
Chr22:38120428..38120429 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.1195C>G (p.Arg399Gly) single nucleotide variant Deafness, autosomal recessive 28 [RCV001337105] Chr22:37723751 [GRCh38]
Chr22:38119758 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3214C>G (p.Arg1072Gly) single nucleotide variant Deafness, autosomal recessive 28 [RCV001337106] Chr22:37725770 [GRCh38]
Chr22:38121777 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.4483G>T (p.Glu1495Ter) single nucleotide variant Deafness, autosomal recessive 28 [RCV001337108] Chr22:37734819 [GRCh38]
Chr22:38130826 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6632A>T (p.Gln2211Leu) single nucleotide variant Deafness, autosomal recessive 28 [RCV001337109] Chr22:37769084 [GRCh38]
Chr22:38165091 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6324+204G>T single nucleotide variant Deafness, autosomal recessive 28 [RCV001329529] Chr22:37759468 [GRCh38]
Chr22:38155475 [GRCh37]
Chr22:22q13.1
pathogenic
NM_001039141.3(TRIOBP):c.5788C>T (p.Arg1930Trp) single nucleotide variant not specified [RCV001449776] Chr22:37757713 [GRCh38]
Chr22:38153720 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6248G>A (p.Arg2083His) single nucleotide variant not specified [RCV001449777] Chr22:37759188 [GRCh38]
Chr22:38155195 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.3910C>T (p.Arg1304Cys) single nucleotide variant Hearing impairment [RCV001375117] Chr22:37726466 [GRCh38]
Chr22:38122473 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.6049G>C (p.Asp2017His) single nucleotide variant Hearing impairment [RCV001375397] Chr22:37757974 [GRCh38]
Chr22:38153981 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.2297dup (p.Asn767fs) duplication Hearing impairment [RCV001375140] Chr22:37724852..37724853 [GRCh38]
Chr22:38120859..38120860 [GRCh37]
Chr22:22q13.1
likely pathogenic
NM_001039141.3(TRIOBP):c.5476A>C (p.Thr1826Pro) single nucleotide variant Hearing impairment [RCV001375396] Chr22:37754973 [GRCh38]
Chr22:38150980 [GRCh37]
Chr22:22q13.1
uncertain significance
NM_001039141.3(TRIOBP):c.1866T>C (p.Asp622=) single nucleotide variant not provided [RCV001471493] Chr22:37724422 [GRCh38]
Chr22:38120429 [GRCh37]
Chr22:22q13.1
likely benign
NM_001039141.3(TRIOBP):c.6849+1G>T single nucleotide variant not provided [RCV001377256] Chr22:37769376 [GRCh38]
Chr22:38165383 [GRCh37]
Chr22:22q13.1
likely pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17009 AgrOrtholog
COSMIC TRIOBP COSMIC
Ensembl Genes ENSG00000100106 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000340312 UniProtKB/TrEMBL
  ENSP00000383913 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000386026 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000387881 UniProtKB/TrEMBL
  ENSP00000396946 UniProtKB/TrEMBL
  ENSP00000399006 UniProtKB/TrEMBL
  ENSP00000400680 UniProtKB/TrEMBL
  ENSP00000407542 UniProtKB/TrEMBL
  ENSP00000496394 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000344404 UniProtKB/TrEMBL
  ENST00000403663 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000407319 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000413051 UniProtKB/TrEMBL
  ENST00000417857 UniProtKB/TrEMBL
  ENST00000418339 UniProtKB/TrEMBL
  ENST00000428075 UniProtKB/TrEMBL
  ENST00000452519 UniProtKB/TrEMBL
  ENST00000644935 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000100106 GTEx
HGNC ID HGNC:17009 ENTREZGENE
Human Proteome Map TRIOBP Human Proteome Map
InterPro M-RIP_PH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:11078 UniProtKB/Swiss-Prot
NCBI Gene 11078 ENTREZGENE
OMIM 609761 OMIM
  609823 OMIM
Pfam PF00169 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142670699 PharmGKB
PROSITE PH_DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00233 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1S5UZ31_HUMAN UniProtKB/TrEMBL
  F6TR96_HUMAN UniProtKB/TrEMBL
  F6WMF4_HUMAN UniProtKB/TrEMBL
  F6WYE2_HUMAN UniProtKB/TrEMBL
  H0Y5J9_HUMAN UniProtKB/TrEMBL
  H0Y5T8_HUMAN UniProtKB/TrEMBL
  H7BXW4_HUMAN UniProtKB/TrEMBL
  Q9H2D6 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B1AHD4 UniProtKB/Swiss-Prot
  B1AHD7 UniProtKB/Swiss-Prot
  F2Z2W0 UniProtKB/Swiss-Prot
  F8W6V6 UniProtKB/Swiss-Prot
  O94797 UniProtKB/Swiss-Prot
  Q2PZW8 UniProtKB/Swiss-Prot
  Q2Q3Z9 UniProtKB/Swiss-Prot
  Q2Q400 UniProtKB/Swiss-Prot
  Q5R3M6 UniProtKB/Swiss-Prot
  Q96DW1 UniProtKB/Swiss-Prot
  Q9BT77 UniProtKB/Swiss-Prot
  Q9BTL7 UniProtKB/Swiss-Prot
  Q9BY98 UniProtKB/Swiss-Prot
  Q9Y3L4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-25 TRIOBP  TRIO and F-actin binding protein  DFNB28  deafness, autosomal recessive 28  Data Merged 737654 PROVISIONAL
2011-08-23 TRIOBP  TRIO and F-actin binding protein  TRIOBP  TRIO and F-actin binding protein  Symbol and/or name change 5135510 APPROVED