Variant #0000304922 (NC_000017.10:g.2577381_2577382del, NM_000430.3:c.699_700del (PAFAH1B1))

Chromosome 17
Allele Unknown
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.2577381_2577382del
DNA change (hg38) g.2674087_2674088del
Published as PAFAH1B1(NM_000430.3):c.699_700delCA (p.H233Qfs*22)
ISCN -
DB-ID PAFAH1B1_000015
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) Retrieve
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 2020-07-10 18:36:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAFAH1B1 NM_000430.3 +/. - c.699_700del r.(?) p.(His233GlnfsTer22)


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