Variant #0000224530 (NC_000005.9:g.155756499C>A, NC_000005.9(NM_000337.5):c.-43-45C>A (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.155756499C>A
DNA change (hg38) g.156329489C>A
Published as -43-45A>C
ISCN -
DB-ID SGCD_000029
Variant remarks -
Reference PubMed: Love
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 4/15
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 15:33:26 +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 -/. 1i c.-43-45C>A r.(=) p.(=)



Screenings

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