Variant #0000614676 (NC_000013.10:g.73349350A>G, NM_006346.2:c.-7185A>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.73349350A>G
DNA change (hg38) g.72775212A>G
Published as DIS3(NM_001128226.1):c.896T>C (p.(Met299Thr))
ISCN -
DB-ID DIS3_000002
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) 0.00247 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIBF1 NM_006346.2 -?/. - c.-7185A>G r.(?) p.(=)
DIS3 NM_014953.3 -?/. - c.986T>C r.(?) p.(Met329Thr)
BORA NM_024808.2 -?/. - c.*19996A>G r.(=) p.(=)


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