Variant #0000321452 (NC_000010.10:g.22607644T>G, NM_005180.8:c.-3001T>G (BMI1))

Chromosome 10
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.22607644T>G
DNA change (hg38) g.22318715T>G
Published as COMMD3(NM_012071.3):c.411+2T>G (p.?)
ISCN -
DB-ID BMI1_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) 4.0E-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 2020-06-26 13:56:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMMD3-BMI1 NM_001204062.1 ?/. - c.351-244T>G r.(=) p.(=)
BMI1 NM_005180.8 ?/. - c.-3001T>G r.(?) p.(=)
COMMD3 NM_012071.3 ?/. - c.411+2T>G r.spl? p.?


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