Variant #0000656144 (NC_000008.10:g.67590151C>T, NM_001033578.2:c.-35039C>T (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.67590151C>T
DNA change (hg38) g.66677916C>T
Published as C8orf44(NM_019607.2):c.208C>T (p.(Arg70Ter))
ISCN -
DB-ID C8orf44_000005
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) 0.00754 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-23 20:20:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGK3 NM_001033578.2 -?/. - c.-35039C>T r.(?) p.(=)
C8orf44-SGK3 NM_001204173.1 -?/. - c.-481-1805C>T r.(=) p.(=)
C8orf44 NM_019607.2 -?/. - c.208C>T r.(?) p.(Arg70Ter)


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