Variant #0000991051 (NC_000001.10:g.243828095T>C, NM_006642.3:c.*165008T>C (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.243828095T>C
DNA change (hg38) -
Published as AKT3(NM_005465.4):c.263A>G (p.(His88Arg))
ISCN -
DB-ID SDCCAG8_000086
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
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.263A>G r.(?) p.(His88Arg)
SDCCAG8 NM_006642.3 ?/. - c.*165008T>C r.(=) p.(=)
AKT3 NM_181690.2 ?/. - c.263A>G r.(?) p.(His88Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.