Variant #0000323989 (NC_000015.9:g.40545082C>T, NM_001211.5:c.*32122C>T (BUB1B))

Chromosome 15
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.40545082C>T
DNA change (hg38) g.40252881C>T
Published as C15orf56(NM_001039905.2):c.8G>A (p.(Arg3His))
ISCN -
DB-ID C15orf56_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C15orf56 NM_001039905.1 ?/. - c.8G>A r.(?) p.(Arg3His)
PAK6 NM_001128628.1 ?/. - c.-117-297C>T r.(=) p.(=)
BUB1B NM_001211.5 ?/. - c.*32122C>T r.(=) p.(=)


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