RGD:150336699 Rat Genome Database

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Variant: RGD:150336699 -  Homo sapiens

RGD ID: 150336699
RS ID: rs4646690
ClinVar ID: CV1172667
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALDH1A3  ALDH1A3-AS1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 101,455,009
GRCh38 15 100,914,804
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000693.4:c.*31G>C
NM_001293815.2:c.*31G>C
NG_012254.1:g.40001G>C
NG_052791.1:g.788G>C
More... 		08/03/2018 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ALDH1A3
Accession:NM_000693
Location:3UTRS;EXON

Gene Symbol:ALDH1A3
Accession:NM_001293815
Location:3UTRS;EXON

Gene Symbol:ALDH1A3-AS1
Accession:NR_135828
Location:EXON;NON-CODING

Gene Symbol:ALDH1A3-AS1
Accession:NR_135831
Location:EXON;NON-CODING

Gene Symbol:ALDH1A3-AS1
Accession:NR_135827
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001541122 CLINVAR
dbSNP (RS) rs4646690 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ALDH1A3 CLINVAR
  ALDH1A3-AS1 CLINVAR
OMIM 600463 CLINVAR