RGD:11614427 Rat Genome Database

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Variant: RGD:11614427 -  Homo sapiens

RGD ID: 11614427
RS ID: rs3473
ClinVar ID: CV332289
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDK4  TSPAN31  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 58,141,938
GRCh38 12 57,748,155
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000075.3:c.*370T>G
LRG_490:g.9227T>G
NG_007484.2:g.9227T>G
NC_000012.12:g.57748155A>C
More... 		01/13/2018 3 prime utr variant benign Cutaneous malignant melanoma 3
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TSPAN31
Accession:NM_001330168
Location:3UTRS;EXON

Gene Symbol:TSPAN31
Accession:XM_024449123
Location:3UTRS;EXON

Gene Symbol:CDK4
Accession:NM_000075
Location:3UTRS;EXON

Gene Symbol:TSPAN31
Accession:NM_001330169
Location:3UTRS;EXON

Gene Symbol:TSPAN31
Accession:NM_005981
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000276725 CLINVAR
dbSNP (RS) rs3473 CLINVAR
MedGen C1836892 CLINVAR
NCBI Gene CDK4 CLINVAR
  TSPAN31 CLINVAR
OMIM 123829 CLINVAR
  181035 CLINVAR
  609048 CLINVAR