Variant #0000689012 (NC_000003.11:g.20225256G>A, NM_138484.3:c.183C>T (SGOL1))

Chromosome 3
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.20225256G>A
DNA change (hg38) -
Published as SGO1(NM_001199251.3):c.183C>T (p.N61=)
ISCN -
DB-ID SGOL1_000004
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.183C>T r.(?) p.(Asn61=)
SGOL1 NM_138484.3 -?/. - c.183C>T r.(?) p.(Asn61=)
SGOL1-AS1 NR_046723.1 -?/. - n.367-2211G>A r.(?) -


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