Variant #0000403832 (NC_000010.10:g.112349704_112349706del, NM_005445.3:c.1464_1466del (SMC3))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.112349704_112349706del
DNA change (hg38) g.110589946_110589948del
Published as -
ISCN -
DB-ID SMC3_000001 See all 2 reported entries
Variant remarks increased affinity of SMC hinge dimers for DNA binding
Reference PubMed: Revenkova 2009, OMIM:var0001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-09-05 15:31:35 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMC3 NM_005445.3 +/. 15 c.1464_1466del r.(?) p.Glu488del


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