Variant #0000403894 (NC_000023.10:g.53449468T>G, NM_006306.2:c.82A>C (SMC1A))

Chromosome X
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.53449468T>G
DNA change (hg38) g.53422519T>G
Published as -
ISCN -
DB-ID SMC1A_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34530151
Origin Germline
Segregation -
Frequency 0.00-0.10
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 2009-09-04 16:50:35 +02:00 (CEST)
Date last edited 2020-07-20 09:57:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMC1A NM_006306.2 ?/? 1 c.82A>C r.(?) p.Thr28Pro


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