Variant #0000001193 (NC_000002.11:g.219135278C>T, PNKD(NM_015488.4):c.20C>T)

Individual ID 00001193
Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.219135278C>T
Reference Liang S1, Yu X2, Zhang S2, Tai J2.(2015)
DB-ID PNKD_000002 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
PNKD NM_015488.4 ./. 1 c.20C>T r.(?) p.(Ala7Val) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001193 ? ? PNKD 1 Y Yang