Variant #0000567366 (NC_000019.9:g.40762915G>A, NM_001626.4:c.93C>T (AKT2))

Chromosome 19
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.40762915G>A
DNA change (hg38) g.40257008G>A
Published as AKT2(NM_001243027.1):c.-94C>T (p.(=)), AKT2(NM_001626.5):c.93C>T (p.S31=), AKT2(NM_001626.6):c.93C>T (p.S31=)
ISCN -
DB-ID AKT2_000002 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) 0.00359 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT2 NM_001626.4 -/. - c.93C>T r.(?) p.(Ser31=)


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