Variant #0000002936 (NC_000007.14:g.877896A>G, NM_001079653.2:c.383A>G (SDK1))

Individual ID 00000713
Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.877896A>G
Published as -
Reference Adiratna Mat Ripen et al.(2020)
DB-ID SDK1_000002 See all 2 reported entries
dbSNP ID rs671694
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-06-27 14:15:37 +08:00 (CST)
Date last edited 2021-08-01 13:11:55 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
SDK1 NM_001079653.2 ?/. 7 c.383A>G - r.(?) p.(His128Arg) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000797 DNA PCR;SEQ SDK1 2 Nur Aisyah Athirah