RGD:14717137 Rat Genome Database

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Variant: RGD:14717137 -  Homo sapiens

RGD ID: 14717137
RS ID: rs2789750
ClinVar ID: CV664591
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TPM2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 35,683,473
GRCh38 9 35,683,476
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.35683476C>G
NM_001301226.2:c.772+770G>C
NM_213674.1:c.772+770G>C
LRG_680t2:c.773-235G>C
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TPM2
Accession:XM_047423827
Location:INTRON

Gene Symbol:TPM2
Accession:XM_017015088
Location:INTRON

Gene Symbol:TPM2
Accession:NM_001301226
Location:INTRON

Gene Symbol:TPM2
Accession:NM_003289
Location:INTRON

Gene Symbol:TPM2
Accession:NM_001301227
Location:INTRON

Gene Symbol:TPM2
Accession:NM_213674
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829964 CLINVAR
dbSNP (RS) rs2789750 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TPM2 CLINVAR
OMIM 190990 CLINVAR