Variant #0001039734 (NC_000013.10:g.73396034T>G, NM_006346.2:c.720T>G (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.73396034T>G
DNA change (hg38) -
Published as PIBF1(NM_006346.4):c.720T>G (p.(Cys240Trp))
ISCN -
DB-ID DIS3_000022
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
PIBF1 NM_006346.2 ?/. - c.720T>G r.(?) p.(Cys240Trp)
DIS3 NM_014953.3 ?/. - c.-40064A>C r.(?) p.(=)


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