RGD:14729736 Rat Genome Database

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Variant: RGD:14729736 -  Homo sapiens

RGD ID: 14729736
RS ID: rs141771518
ClinVar ID: CV664164
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL5A1  LOC127816663  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 137,676,636
GRCh38 9 134,784,790
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001278074.1:c.2485-199G>A
NG_008030.1:g.147985G>A
NC_000009.12:g.134784790G>A
NC_000009.11:g.137676636G>A
More... 		06/20/2018 intron variant likely 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 RCV000835356 CLINVAR
dbSNP (RS) rs141771518 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL5A1 CLINVAR
OMIM 120215 CLINVAR