Variant #0000506695 (NC_000001.10:g.243581286G>A, NM_006642.3:c.1761G>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.243581286G>A
DNA change (hg38) g.243417984G>A
Published as SDCCAG8(NM_006642.4):c.1761G>A (p.L587=)
ISCN -
DB-ID SDCCAG8_000037
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) 0.0005 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.*87265C>T r.(=) p.(=)
SDCCAG8 NM_006642.3 -?/. - c.1761G>A r.(?) p.(Leu587=)
AKT3 NM_181690.2 -?/. - c.*70473C>T r.(=) p.(=)


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