Variant #0000724574 (NC_000013.10:g.73396066_73396070del, NM_006346.2:c.752_756del (PIBF1))

Chromosome 13
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.73396066_73396070del
DNA change (hg38) -
Published as PIBF1(NM_006346.4):c.752_756delAACAG (p.K251Ifs*6)
ISCN -
DB-ID DIS3_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIBF1 NM_006346.2 +/. - c.752_756del r.(?) p.(Lys251IlefsTer6)
DIS3 NM_014953.3 +/. - c.-40100_-40096del r.(?) p.(=)


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