Variant #0000620591 (NC_000001.10:g.243480091G>A, NM_006642.3:c.964G>A (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.243480091G>A
DNA change (hg38) g.243316789G>A
Published as SDCCAG8(NM_001350251.1):c.61G>A (p.V21I)
ISCN -
DB-ID SDCCAG8_000043
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) 9.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 ?/. - c.*188460C>T r.(=) p.(=)
SDCCAG8 NM_006642.3 ?/. - c.964G>A r.(?) p.(Val322Ile)
AKT3 NM_181690.2 ?/. - c.*171668C>T r.(=) p.(=)


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