RGD:150417154 Rat Genome Database

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Variant: RGD:150417154 -  Homo sapiens

RGD ID: 150417154
RS ID: rs116699817
ClinVar ID: CV1181860
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADA  LOC107303343  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 43,264,784
GRCh38 20 44,636,143
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001322050.2:c.-195+84G>A
NM_000022.4:c.95+84G>A
NM_001322051.2:c.95+84G>A
LRG_16:g.20593G>A
More... 		09/02/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ADA
Accession:NM_001322050
Location:5UTRS;INTRON

Gene Symbol:ADA
Accession:NM_000022
Location:INTRON

Gene Symbol:ADA
Accession:NM_001322051
Location:INTRON

Gene Symbol:ADA
Accession:NR_136160
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001549993 CLINVAR
dbSNP (RS) rs116699817 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ADA CLINVAR
  LOC107303343 CLINVAR
OMIM 608958 CLINVAR