RGD:14733962 Rat Genome Database

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Variant: RGD:14733962 -  Homo sapiens

RGD ID: 14733962
RS ID: rs3211620
ClinVar ID: CV666812
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDK4  TSPAN31  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 58,143,445
GRCh38 12 57,749,662
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001330168.2:c.*2372T>C
NM_001330169.2:c.*2372T>C
NM_005981.5:c.*2372T>C
NM_000075.4:c.633-158A>G
More... 		06/18/2018 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TSPAN31
Accession:NM_001330169
Location:3UTRS;EXON

Gene Symbol:TSPAN31
Accession:NM_001330168
Location:3UTRS;EXON

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

Gene Symbol:CDK4
Accession:NM_000075
Location:INTRON

Gene Symbol:TSPAN31
Accession:XM_024449123
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000837337 CLINVAR
dbSNP (RS) rs3211620 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CDK4 CLINVAR
  TSPAN31 CLINVAR
OMIM 123829 CLINVAR
  181035 CLINVAR