Variant #0001000619 (NC_000013.10:g.73334740_73334745del, NM_006346.2:c.-21795_-21790del (PIBF1))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.73334740_73334745del
DNA change (hg38) -
Published as DIS3(NM_014953.3):c.2721_2726delTAAAGT (p.(Lys908_Val909del))
ISCN -
DB-ID DIS3_000021
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MZT1 NM_001071775.2 ?/. - c.-32999_-32994del r.(?) p.(=)
PIBF1 NM_006346.2 ?/. - c.-21795_-21790del r.(?) p.(=)
DIS3 NM_014953.3 ?/. - c.2721_2726del r.(?) p.(Val909_Lys910del)
BORA NM_024808.2 ?/. - c.*5386_*5391del r.(=) p.(=)


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