Variant #0000001109 (NC_000002.11:g.219136133G>C, PNKD(NM_015488.4):c.97G>C)

Individual ID 00001109
Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.219136133G>C
Reference Ghezzi D1, Viscomi C, Ferlini A, Gualandi F, Mereghetti P, DeGrandis D, Zeviani M.(2009)
DB-ID PNKD_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00063 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
PNKD NM_015488.4 ./. 2 c.97G>C r.(?) p.(Ala33Pro) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001109 ? ? PNKD 1 Y Yang