RGD:150413160 Rat Genome Database

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Variant: RGD:150413160 -  Homo sapiens

RGD ID: 150413160
RS ID: rs140919896
ClinVar ID: CV1177697
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL4A2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 13 111,081,237
GRCh38 13 110,428,890
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.477+307G>A
NG_032137.1:g.126607G>A
NC_000013.11:g.110428890G>A
NC_000013.10:g.111081237G>A
 07/10/2018 intron variant likely benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001547711 CLINVAR
dbSNP (RS) rs140919896 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL4A2 CLINVAR
OMIM 120090 CLINVAR