Variant #0000311619 (NC_000012.11:g.56398454G>C, NM_001032386.1:c.1281G>C (SUOX))

Chromosome 12
Allele Unknown
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.56398454G>C
DNA change (hg38) g.56004670G>C
Published as SUOX(NM_000456.3):c.1281G>C (p.S427=)
ISCN -
DB-ID SUOX_000007 See all 2 reported entries
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) 0.88527 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUOX NM_001032386.1 -/. 5 c.1281G>C r.(?) p.(Ser427=)
IKZF4 NM_022465.3 -/. - c.-16824G>C r.(?) p.(=)


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