RGD:14726737 Rat Genome Database

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Variant: RGD:14726737 -  Homo sapiens

RGD ID: 14726737
RS ID: rs7855838
ClinVar ID: CV663444
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL5A1  LOC127816663  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 137,676,644
GRCh38 9 134,784,798
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.2485-191C>A
NG_008030.1:g.147993C>A
NC_000009.12:g.134784798C>A
NC_000009.11:g.137676644C>A
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:COL5A1
Accession:XM_017014266
Location:INTRON

Gene Symbol:COL5A1
Accession:NM_001278074
Location:INTRON

Gene Symbol:COL5A1
Accession:NM_000093
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000833999 CLINVAR
dbSNP (RS) rs7855838 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL5A1 CLINVAR
OMIM 120215 CLINVAR