RGD:150464485 Rat Genome Database

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Variant: RGD:150464485 -  Homo sapiens

RGD ID: 150464485
RS ID: rs74191879
ClinVar ID: CV1241301
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAM20C  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 298,844
GRCh38 7 258,878
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020223.4:c.1505+173C>A
NC_000007.14:g.258878C>A
NG_033970.1:g.68514C>A
NC_000007.13:g.298844C>A
 03/28/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FAM20C
Accession:XM_047420625
Location:INTRON

Gene Symbol:FAM20C
Accession:NM_020223
Location:INTRON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001649812 CLINVAR
dbSNP (RS) rs74191879 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FAM20C CLINVAR
OMIM 611061 CLINVAR