Variant #0000857405 (NC_000001.10:g.243727130G>A, NM_006642.3:c.*64043G>A (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.243727130G>A
DNA change (hg38) -
Published as AKT3(NM_005465.5):c.840C>T (p.D280=)
ISCN -
DB-ID SDCCAG8_000071
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) 8.0E-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 2022-05-09 15:51:19 +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.840C>T r.(?) p.(Asp280=)
SDCCAG8 NM_006642.3 -?/. - c.*64043G>A r.(=) p.(=)
AKT3 NM_181690.2 -?/. - c.840C>T r.(?) p.(Asp280=)


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