Variant #0000261739 (NC_000020.10:g.25284273G>A, NC_000020.10(NM_001042472.2):c.951-9C>T (ABHD12))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25284273G>A
DNA change (hg38) g.25303637G>A
Published as ABHD12(NM_001042472.3):c.951-9C>T
ISCN -
DB-ID ABHD12_000014
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12 NM_001042472.2 -?/. - c.951-9C>T r.(=) p.(=)
PYGB NM_002862.3 -?/. - c.*7115G>A r.(=) p.(=)


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