Variant #0000329289 (NC_000003.11:g.20225528T>C, NC_000003.11(NM_138484.3):c.-7-2A>G (SGOL1))

Chromosome 3
Allele Unknown
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.20225528T>C
DNA change (hg38) g.20184036T>C
Published as SGOL1(NM_001199251.1):c.-7-2A>G (p.(=))
ISCN -
DB-ID SGOL1_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGOL1 NM_001199251.1 ?/. - c.-7-2A>G r.spl? p.?
SGOL1 NM_138484.3 ?/. - c.-7-2A>G r.spl? p.?
SGOL1-AS1 NR_046723.1 ?/. - n.367-1939T>C r.(?) -


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