Variant #0000002915 (NC_000008.11:g.64752G>A, NM_014265.6:c.2293G>A (ADAM28))

Individual ID 00000713
Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.64752G>A
Published as -
Reference Adiratna Mat Ripen et al.(2020)
DB-ID ADAM28_000001 See all 2 reported entries
dbSNP ID rs7814768
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 12:09:40 +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     
ADAM28 NM_014265.6 -/. 22 c.2293G>A - r.(?) p.(Val765Met) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000795 DNA PCR;SEQ ADAM28 1 Nur Aisyah Athirah