Variant #0000891563 (NC_000013.10:g.73357758A>G, NM_006346.2:c.151A>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.73357758A>G
DNA change (hg38) -
Published as PIBF1(NM_006346.3):c.151A>G (p.I51V)
ISCN -
DB-ID DIS3_000012
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) 0.00196 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 2022-11-01 13:01:21 +01:00 (CET)
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.151A>G r.(?) p.(Ile51Val)
DIS3 NM_014953.3 -?/. - c.-1788T>C r.(?) p.(=)
BORA NM_024808.2 -?/. - c.*28404A>G r.(=) p.(=)


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