Variant #0000223301 (NC_000005.9:g.155922099C>T, NC_000005.9(NM_000337.5):c.193-13512C>T (SGCD))

Chromosome 5
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.155922099C>T
DNA change (hg38) g.156495089C>T
Published as -
ISCN -
DB-ID SGCD_000015
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1368300
Origin Germline
Segregation -
Frequency 0.22
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 2005-01-15 14:57:07 +01:00 (CET)
Date last edited 2012-11-02 20:43:04 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCD NM_000337.5 -/. 3i c.193-13512C>T r.(=) p.(=)


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