RGD:150470600 Rat Genome Database

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Variant: RGD:150470600 -  Homo sapiens

RGD ID: 150470600
RS ID: rs4577908
ClinVar ID: CV1258617
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAM20C  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 192,800
GRCh38 7 192,800
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.-400G>A
NG_033970.1:g.4832G>A
NC_000007.14:g.192800G>A
NC_000007.13:g.192800G>A
 04/27/2021 5 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FAM20C
Accession:NM_020223
Location:5UTRS;EXON

Gene Symbol:FAM20C
Accession:XM_047420625
Location:5UTRS;EXON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001684162 CLINVAR
dbSNP (RS) rs4577908 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FAM20C CLINVAR
OMIM 611061 CLINVAR