rs117638434 Rat Genome Database

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Variant: rs117638434 -  Homo sapiens

RGD ID: 11546848
RS ID: rs117638434
ClinVar ID: CV255160
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDIN1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 36,989,578
GRCh38 15 36,697,377
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_034055.1:g.122775C>T
NC_000015.10:g.36697377C>T
NC_000015.9:g.36989578C>T
NP_001123482.1:p.Asn177=
More... 		03/01/2023 synonymous variant benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:CDIN1
Accession:NM_001130010
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 177
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MILTKAQYDEIAQCLVSVPPTRQSLRKLKQRFPSQSQATLLSIFSQEYQKHIKRTHAKHHTSEAIESYYQRYLNGVVKNG
AAPVLLDLANEVDYAPSLMARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHA
IGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRF
GPGLVIYWYGFIQELDCNRERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_032499
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 79
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNL
SFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCN
RERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_001290233
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 177
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MILTKAQYDEIAQCLVSVPPTRQSLRKLKQRFPSQSQATLLSIFSQEYQKHIKRTHAKHHTSEAIESYYQRYLNGVVKNG
AAPVLLDLANEVDYAPSLMARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHA
IGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRD
GISQCSSGWCGTPGLSDSSASATQSAGITGARKHFLPGIFMKCVCK*

Gene Symbol:CDIN1
Accession:NM_001290232
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 79
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNL
SFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCN
RERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_001321757
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 54
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPV
AVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCNRERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_001321761
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 177
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MILTKAQYDEIAQCLVSVPPTRQSLRKLKQRFPSQSQATLLSIFSQEYQKHIKRTHAKHHTSEAIESYYQRYLNGVVKNG
AAPVLLDLANEVDYAPSLMARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHA
IGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPVVMLCPLAVEGHIIHWIESKASFGDECSHHAYLHDQFW
SYWNRFGPGLVIYWYGFIQELDCNRERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_001321759
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 177
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MILTKAQYDEIAQCLVSVPPTRQSLRKLKQRFPSQSQATLLSIFSQEYQKHIKRTHAKHHTSEAIESYYQRYLNGVVKNG
AAPVLLDLANEVDYAPSLMARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHA
IGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRF
GPGLVIYWYGFIQELDCNRERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_001321760
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 177
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MILTKAQYDEIAQCLVSVPPTRQSLRKLKQRFPSQSQATLLSIFSQEYQKHIKRTHAKHHTSEAIESYYQRYLNGVVKNG
AAPVLLDLANEVDYAPSLMARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHA
IGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPVDLGQA*

Gene Symbol:CDIN1
Accession:NM_001321756
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 79
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNL
SFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCN
RERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:NM_001321758
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 140
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MILTKAQYDEIAQCLVSVPPTRQSLRKLKQRFPRYLNGVVKNGAAPVLLDLANEVDYAPSLMARLILERFLQEHEETPPS
KSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDF
ILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCNRERGILLKACFPTNIVTLC
HSIA*

Gene Symbol:CDIN1
Accession:XM_047433174
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 79
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLILERFLQEHEETPPSKSIINSMLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNL
SFLDEDQLRAKGYDKTPDFILQVPVAVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCN
RERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:XM_047433176
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 54
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLRDPSQIPDGVLANQVYQCIVNDCCYGPLVDCIKHAIGHEHEVLLRDLLLEKNLSFLDEDQLRAKGYDKTPDFILQVPV
AVEGHIIHWIESKASFGDECSHHAYLHDQFWSYWNRFGPGLVIYWYGFIQELDCNRERGILLKACFPTNIVTLCHSIA*

Gene Symbol:CDIN1
Accession:XM_017022676
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_017022677
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433171
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433172
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433173
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433175
Location:INTRON

Gene Symbol:CDIN1
Accession:XR_007064491
Location:INTRON;NON-CODING

Gene Symbol:CDIN1
Accession:XR_007064492
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000246997 CLINVAR
  RCV002229951 CLINVAR
dbSNP (RS) rs117638434 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene C15orf41 CLINVAR
OMIM 615626 CLINVAR