RGD:150422334 Rat Genome Database

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Variant: RGD:150422334 -  Homo sapiens

RGD ID: 150422334
RS ID: rs191089093
ClinVar ID: CV1181843
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ABHD12  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 25,288,577
GRCh38 20 25,307,941
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001042472.3:c.867+25T>A
NM_015600.5:c.867+25T>A
NG_028119.1:g.88042T>A
NC_000020.11:g.25307941A>T
More...
07/26/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ABHD12
Accession:NM_015600
Location:INTRON

Gene Symbol:ABHD12
Accession:NM_001042472
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_011529214
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_017027797
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440090
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440093
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440089
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440087
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440092
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440094
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440091
Location:INTRON

Gene Symbol:ABHD12
Accession:XM_047440088
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001552511 CLINVAR
dbSNP (RS) rs191089093 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ABHD12 CLINVAR
OMIM 613599 CLINVAR