Variant #0000260050 (NC_000001.10:g.243776987C>T, NM_006642.3:c.*113900C>T (SDCCAG8))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.243776987C>T
DNA change (hg38) g.243613685C>T
Published as AKT3(NM_005465.7):c.682G>A (p.V228I)
ISCN -
DB-ID AKT3_000009
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 +?/. - c.682G>A r.(?) p.(Val228Ile)
SDCCAG8 NM_006642.3 +?/. - c.*113900C>T r.(=) p.(=)
AKT3 NM_181690.2 +?/. - c.682G>A r.(?) p.(Val228Ile)


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