Variant #0000569271 (NC_000020.10:g.25371112_25371113insCCCCCCCCCCCCCCCCCCCCC, ABHD12(NM_001042472.2):c.191+36_191+37insGGGGGGGGGGGGGGGGGGGGG)

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.25371112_25371113insCCCCCCCCCCCCCCCCCCCCC
DNA change (hg38) g.25390476_25390477insCCCCCCCCCCCCCCCCCCCCC
Published as ABHD12(NM_001042472.3):c.191+31_191+36delGGGGGCinsGGGGGCGGGGGGGGGGGGGGGGGGGGG
ISCN -
DB-ID PYGB_000027
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) Variant not found in online data sets
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12 NM_001042472.2 -?/. - c.191+36_191+37insGGGGGGGGGGGGGGGGGGGGG r.(=) p.(=)
PYGB NM_002862.3 -?/. - c.*93954_*93955insCCCCCCCCCCCCCCCCCCCCC r.(=) p.(=)