Variant #0000911021 (NC_000001.10:g.243437831A>T, NC_000001.10(NM_006642.3):c.307-14A>T (SDCCAG8))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.243437831A>T
DNA change (hg38) -
Published as SDCCAG8(NM_001350251.2):c.-1067-14A>T
ISCN -
DB-ID SDCCAG8_000082
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +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.*230720T>A r.(=) p.(=)
SDCCAG8 NM_006642.3 -?/. - c.307-14A>T r.(=) p.(=)
AKT3 NM_181690.2 -?/. - c.*213928T>A r.(=) p.(=)


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