RGD:10053473 Rat Genome Database

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Variant: RGD:10053473 -  Homo sapiens

RGD ID: 10053473
RS ID: rs794727975
ClinVar ID: CV196314
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAM20C  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 298,676
GRCh38 7 258,710
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.258710A>G
NC_000007.13:g.298676A>G
NM_020223.4:c.1505+5A>G
NG_033970.1:g.68346A>G
04/23/2015 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:FAM20C
Accession:NM_020223
Location:INTRON

Gene Symbol:FAM20C
Accession:XM_047420625
Location:INTRON

Gene Symbol:FAM20C
Accession:XR_007060117
Location:INTRON;NON-CODING

Gene Symbol:FAM20C
Accession:XR_007060116
Location:INTRON;NON-CODING

Gene Symbol:FAM20C
Accession:XR_001744837
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000180669 CLINVAR
dbSNP (RS) rs794727975 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene FAM20C CLINVAR
OMIM 611061 CLINVAR