Variant #0000223355 (NC_000008.10:g.15095332A>G, NM_139167.2:c.-200T>C (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.15095332A>G
DNA change (hg38) g.15237823A>G
Published as -
ISCN -
DB-ID SGCZ_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs11782191
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 ?/. 1 c.-200T>C r.(?) p.(=)


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