Variant #0000403831 (NC_000010.10:g.112361870A>G, NM_005445.3:c.3039A>G (SMC3))

Chromosome 10
Allele Parent #1
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.112361870A>G
DNA change (hg38) g.110602112A>G
Published as -
ISCN -
DB-ID SMC3_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2419565
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.99685 View details
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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMC3 NM_005445.3 -?/. 25 c.3039A>G r.(?) p.(=)


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