Variant #0000129972 (NC_000020.10:g.25300900C>T, ABHD12(NM_001042472.2):c.447G>A)

Individual ID 00080792
Chromosome 20
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25300900C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABHD12_000008 See all 4 reported entries
Variant remarks Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message.
Reference PubMed: Nishiguchi 2014
ClinVar ID ClinVar-RCV000132768.3
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Lonneke Haer-Wigman
Database submission license No license selected
Created by Lonneke Haer-Wigman
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12 NM_001042472.2 +/. - c.447G>A r.(?) p.(Trp159*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000080904 DNA SEQ-NG - - - 2 Lonneke Haer-Wigman