Variant #0000001481 (NC_000002.12:g.162033665T>A, NC_000002.12(NM_001935.3):c.775-12A>T (DPP4))

Individual ID 00000312
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.162033665T>A
Published as -
Reference Radwan H Ahmed et al. (2016), dbSNP
DB-ID DPP4_000008 See all 2 reported entries
dbSNP ID rs1558957
Frequency 47/314
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-03 08:53:18 +08:00 (CST)
Date last edited 2021-09-01 10:28:01 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
DPP4 NM_001935.3 +/. - c.775-12A>T - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000327 DNA TaqMan DPP4 12 Nuur Athirah Binti Mohd Daud