Variant #0001050503 (NC_000001.10:g.243471462C>T, NM_006642.3:c.912C>T (SDCCAG8))

Chromosome 1
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.243471462C>T
DNA change (hg38) -
Published as SDCCAG8(NM_006642.4):c.912C>T (p.T304=), SDCCAG8(NM_006642.5):c.912C>T (p.(Thr304=))
ISCN -
DB-ID SDCCAG8_000016 See all 3 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) 0.02011 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 -?/. - c.*197089G>A r.(=) p.(=)
SDCCAG8 NM_006642.3 -?/. - c.912C>T r.(?) p.(Thr304=)
AKT3 NM_181690.2 -?/. - c.*180297G>A r.(=) p.(=)


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