Variant #0000001461 (NC_000002.12:g.162029379A>C, NC_000002.12(NM_001935.3):c.887+4162T>G (DPP4))

Individual ID 00000309
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.162029379A>C
Published as -
Reference Radwan H Ahmed et al. (2016), dbSNP
DB-ID DPP4_000002 See all 6 reported entries
dbSNP ID rs4664443
Frequency 30/153
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 2020-12-29 12:39:30 +08:00 (CST)
Date last edited 2021-08-30 15:36:42 +08:00 (CST)
Options




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.887+4162T>G - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000324 DNA TaqMan DPP4 4 Nuur Athirah Binti Mohd Daud