Variant #0001000620 (NC_000013.10:g.73409497G>A, NM_006346.2:c.1214G>A (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.73409497G>A
DNA change (hg38) -
Published as PIBF1(NM_006346.2):c.1214G>A (p.(Arg405Gln)), PIBF1(NM_006346.3):c.1214G>A (p.R405Q)
ISCN -
DB-ID PIBF1_000004 See all 4 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) 0.01459 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 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     
PIBF1 NM_006346.2 -?/. - c.1214G>A r.(?) p.(Arg405Gln)
DIS3 NM_014953.3 -?/. - c.-53527C>T r.(?) p.(=)


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