RGD:150493327 Rat Genome Database

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Variant: RGD:150493327 -  Homo sapiens

RGD ID: 150493327
RS ID: rs76226836
ClinVar ID: CV1267124
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL5A1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 137,709,088
GRCh38 9 134,817,242
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_737t2:c.4176+163T>A
NM_000093.5:c.4176+163T>A
NM_001278074.1:c.4176+163T>A
LRG_737:g.180437T>A
More... 		07/07/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:COL5A1
Accession:NM_001278074
Location:INTRON

Gene Symbol:COL5A1
Accession:XM_017014266
Location:INTRON

Gene Symbol:COL5A1
Accession:NM_000093
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001688151 CLINVAR
dbSNP (RS) rs76226836 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL5A1 CLINVAR
OMIM 120215 CLINVAR