rs11103543 Rat Genome Database

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Variant: rs11103543 -  Homo sapiens

RGD ID: 14710313
RS ID: rs11103543
ClinVar ID: CV664298
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL5A1  LOC101448202  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 137,733,714
GRCh38 9 134,841,868
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001278074.1:c.5371-289T>C
NG_008030.1:g.205063T>C
NC_000009.12:g.134841868T>C
NC_000009.11:g.137733714T>C
More... 		06/19/2018 intron variant benign none provided

Gene Symbol:COL5A1
Accession:NM_000093
Location:INTRON

Gene Symbol:COL5A1
Accession:NM_001278074
Location:INTRON

Gene Symbol:COL5A1
Accession:XM_017014266
Location:INTRON

Gene Symbol:LOC101448202
Accession:NR_103451
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV000827665 CLINVAR
dbSNP (RS) rs11103543 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene 101448202 CLINVAR
  COL5A1 CLINVAR
OMIM 120215 CLINVAR