RGD:150430365 Rat Genome Database

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Variant: RGD:150430365 -  Homo sapiens

RGD ID: 150430365
RS ID: rs4841934
ClinVar ID: CV1230843
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL5A1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 137,707,942
GRCh38 9 134,816,096
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_737t2:c.4122+108T>C
NM_000093.5:c.4122+108T>C
NM_001278074.1:c.4122+108T>C
NC_000009.12:g.134816096T>C
More... 		06/23/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:COL5A1
Accession:NM_000093
Location:INTRON

Gene Symbol:COL5A1
Accession:NM_001278074
Location:INTRON

Gene Symbol:COL5A1
Accession:XM_017014266
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001641392 CLINVAR
dbSNP (RS) rs4841934 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL5A1 CLINVAR
OMIM 120215 CLINVAR