RGD:8635519 Rat Genome Database

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Variant: RGD:8635519 -  Homo sapiens

RGD ID: 8635519
ClinVar ID: CV90740
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALDH1A2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 58,306,374
GRCh38 15 58,014,176
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001206897.1:c.159+1G>A
NM_170696.2:c.222+1G>A
NM_003888.3:c.222+1G>A
NG_012259.1:g.56533G>A
More... 		2kb upstream variant|splice donor variant|splice-5 not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:ALDH1A2
Accession:NM_003888
Location:INTRON

Gene Symbol:ALDH1A2
Accession:NM_170696
Location:INTRON

Gene Symbol:ALDH1A2
Accession:NM_001206897
Location:INTRON

Gene Symbol:ALDH1A2
Accession:NM_170697
Location:INTRON

Variant Samples