Variant #0001024143 (NC_000001.10:g.244006448C>G, NM_006642.3:c.*343361C>G (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.244006448C>G
DNA change (hg38) -
Published as AKT3(NM_005465.7):c.25G>C (p.E9Q)
ISCN -
DB-ID SDCCAG8_000088
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 ?/. - c.25G>C r.(?) p.(Glu9Gln)
SDCCAG8 NM_006642.3 ?/. - c.*343361C>G r.(=) p.(=)
AKT3 NM_181690.2 ?/. - c.25G>C r.(?) p.(Glu9Gln)


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