Variant #0000518931 (NC_000003.11:g.20225127T>G, NM_138484.3:c.312A>C (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.20225127T>G
DNA change (hg38) g.20183635T>G
Published as SGO1(NM_001199251.3):c.312A>C (p.T104=)
ISCN -
DB-ID SGOL1_000002
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) 7.0E-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 2019-07-18 18:22:55 +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.312A>C r.(?) p.(Thr104=)
SGOL1 NM_138484.3 -?/. - c.312A>C r.(?) p.(Thr104=)
SGOL1-AS1 NR_046723.1 -?/. - n.367-2340T>G r.(?) -


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