Variant #0000506705 (NC_000001.10:g.243736227C>T, NM_006642.3:c.*73140C>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.243736227C>T
DNA change (hg38) g.243572925C>T
Published as AKT3(NM_001206729.1):c.819+1G>A (p.?)
ISCN -
DB-ID SDCCAG8_000041
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-06 17:33:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 -?/. - c.819+1G>A r.spl? p.?
SDCCAG8 NM_006642.3 -?/. - c.*73140C>T r.(=) p.(=)
AKT3 NM_181690.2 -?/. - c.819+1G>A r.spl? p.?


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