Variant #0000997299 (NC_000008.10:g.67705993G>A, NM_001033578.2:c.22G>A (SGK3))

Chromosome 8
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.67705993G>A
DNA change (hg38) -
Published as SGK3(NM_001033578.2):c.22G>A (p.(Asp8Asn))
ISCN -
DB-ID C8orf44_000007
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 2024-08-28 13:16:32 +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     
SGK3 NM_001033578.2 -?/. - c.22G>A r.(?) p.(Asp8Asn)
C8orf44-SGK3 NM_001204173.1 -?/. - c.22G>A r.(?) p.(Asp8Asn)
C8orf44 NM_019607.2 -?/. - c.*113804G>A r.(=) p.(=)


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