Variant #0000605588 (NC_000001.10:g.243542168A>T, NC_000001.10(NM_006642.3):c.1616+3A>T (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.243542168A>T
DNA change (hg38) g.243378866A>T
Published as SDCCAG8(NM_006642.4):c.1616+3A>T
ISCN -
DB-ID SDCCAG8_000044
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-06 17:31:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 ?/. - c.*126383T>A r.(=) p.(=)
SDCCAG8 NM_006642.3 ?/. - c.1616+3A>T r.spl? p.?
AKT3 NM_181690.2 ?/. - c.*109591T>A r.(=) p.(=)


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