Variant #0000223359 (NC_000008.10:g.13965719G>A, NM_139167.2:c.573C>T (SGCZ))

Chromosome 8
Allele Parent #1
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.13965719G>A
DNA change (hg38) g.14108210G>A
Published as -
ISCN -
DB-ID SGCZ_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs13277240
Origin Germline
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 2008-02-23 18:19:01 +01:00 (CET)
Date last edited 2012-11-02 20:43:05 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCZ NM_139167.2 ?/. 6 c.573C>T r.(?) p.(=)


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