Variant #0000853699 (NC_000013.10:g.73505365T>G, NM_006346.2:c.1793T>G (PIBF1))

Chromosome 13
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.73505365T>G
DNA change (hg38) -
Published as PIBF1(NM_001349655.1):c.1880T>G (p.L627R), PIBF1(NM_006346.3):c.1793T>G (p.L598R)
ISCN -
DB-ID DIS3_000006 See all 2 reported entries
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) 0.0014 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIBF1 NM_006346.2 -?/. - c.1793T>G r.(?) p.(Leu598Arg)
DIS3 NM_014953.3 -?/. - c.-149395A>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.