Variant #0000539733 (NC_000010.10:g.22608868G>C, NM_005180.8:c.-1777G>C (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.22608868G>C
DNA change (hg38) g.22319939G>C
Published as COMMD3(NM_012071.4):c.529G>C (p.D177H)
ISCN -
DB-ID BMI1_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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
COMMD3-BMI1 NM_001204062.1 ?/. - c.410+921G>C r.(=) p.(=)
BMI1 NM_005180.8 ?/. - c.-1777G>C r.(?) p.(=)
COMMD3 NM_012071.3 ?/. - c.529G>C r.(?) p.(Asp177His)


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