RGD:14745652 Rat Genome Database

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Variant: RGD:14745652 -  Homo sapiens

RGD ID: 14745652
RS ID: rs7933466
ClinVar ID: CV665792
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSRP3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 19,213,606
GRCh38 11 19,192,059
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001369404.1:c.112+278T>C
NM_003476.5:c.112+278T>C
NG_011932.2:g.23515T>C
NC_000011.10:g.19192059A>G
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CSRP3
Accession:NM_001369404
Location:INTRON

Gene Symbol:CSRP3
Accession:NM_003476
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000843600 CLINVAR
dbSNP (RS) rs7933466 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CSRP3 CLINVAR
OMIM 600824 CLINVAR