RGD:15102656 Rat Genome Database

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Variant: RGD:15102656 -  Homo sapiens

RGD ID: 15102656
RS ID: rs376166238
ClinVar ID: CV759543
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAM20C  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 296,966
GRCh38 7 257,000
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.257000C>T
NC_000007.13:g.296966C>T
NM_020223.3:c.1364-5C>T
NM_020223.4:c.1364-5C>T
More...
10/16/2018 intron variant likely 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_007060116
Location:INTRON;NON-CODING

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

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

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000915006 CLINVAR
dbSNP (RS) rs376166238 CLINVAR
MedGen C3661900 CLINVAR
  CN517202 CLINVAR
NCBI Gene FAM20C CLINVAR
OMIM 611061 CLINVAR