Variant #0000848673 (NC_000001.10:g.243778451G>A, NM_006642.3:c.*115364G>A (SDCCAG8))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.243778451G>A
DNA change (hg38) -
Published as AKT3(NM_001206729.1):c.574C>T (p.(His192Tyr))
ISCN -
DB-ID SDCCAG8_000072
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 +?/. - c.574C>T r.(?) p.(His192Tyr)
SDCCAG8 NM_006642.3 +?/. - c.*115364G>A r.(=) p.(=)
AKT3 NM_181690.2 +?/. - c.574C>T r.(?) p.(His192Tyr)


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