Variant #0000997300 (NC_000008.10:g.67726105C>T, NM_001033578.2:c.271C>T (SGK3))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.67726105C>T
DNA change (hg38) -
Published as SGK3(NM_001033578.2):c.271C>T (p.(Arg91*))
ISCN -
DB-ID C8orf44_000008
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) 1.0E-5 View details
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.271C>T r.(?) p.(Arg91*)
C8orf44-SGK3 NM_001204173.1 ?/. - c.271C>T r.(?) p.(Arg91*)
C8orf44 NM_019607.2 ?/. - c.*133916C>T r.(=) p.(=)


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