RGD:150423002 Rat Genome Database

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Variant: RGD:150423002 -  Homo sapiens

RGD ID: 150423002
RS ID: rs73619404
ClinVar ID: CV1181100
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL4A2  COL4A2-AS2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 13 111,109,995
GRCh38 13 110,457,648
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001846.4:c.1432+213G>A
NG_032137.1:g.155365G>A
NC_000013.11:g.110457648G>A
NC_000013.10:g.111109995G>A
 09/18/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:COL4A2
Accession:NM_001846
Location:INTRON

Gene Symbol:COL4A2-AS2
Accession:NR_171022
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001553419 CLINVAR
dbSNP (RS) rs73619404 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL4A2 CLINVAR
  COL4A2-AS2 CLINVAR
OMIM 120090 CLINVAR