Variant #0000223353 (NC_000008.10:g.13947941A>T, NM_139167.2:c.*11T>A (SGCZ))

Chromosome 8
Allele Unknown
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.13947941A>T
DNA change (hg38) g.14090432A>T
Published as -
ISCN -
DB-ID SGCZ_000014
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs73213896
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01384 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 2009-12-18 16:14:36 +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 -?/. 8 c.*11T>A r.(?) p.(=)


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