Variant #0000000732 (NC_000004.12:g.55106807T>A, KDR(NM_002253.3):c.1416A>T)

Individual ID 00000141
Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.55106807T>A
Published as 55972974T>A
Reference Nurul-Syakima Ab Mutalib et al. (2014)dbSNP
DB-ID KDR_000001 See all 2 reported entries
dbSNP ID rs1870377
Frequency 6/9
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
KDR NM_002253.3 ?/. - c.1416A>T - r.(?) p.(Gln472His) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000156 DNA SEQ-NG;PCR KDR 2 Nuur Athirah Binti Mohd Daud