Variant #0000307848 (NC_000001.10:g.243434337C>T, NM_006642.3:c.278C>T (SDCCAG8))

Chromosome 1
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.243434337C>T
DNA change (hg38) g.243271035C>T
Published as SDCCAG8(NM_006642.3):c.278C>T (p.(Pro93Leu)), SDCCAG8(NM_006642.4):c.278C>T (p.P93L), SDCCAG8(NM_006642.5):c.278C>T (p.P93L)
ISCN -
DB-ID SDCCAG8_000008 See all 5 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) 0.001 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 ?/. - c.*234214G>A r.(=) p.(=)
SDCCAG8 NM_006642.3 ?/. - c.278C>T r.(?) p.(Pro93Leu)
AKT3 NM_181690.2 ?/. - c.*217422G>A r.(=) p.(=)


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