Variant #0000000378 (NC_000007.13:g.95034775G>C, PON2(NM_000305.2):c.932C>G)

Individual ID 00000378
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.95034775G>C
Reference Slowik A1, Tomik B, Wolkow PP, Partyka D, Turaj W, Malecki MT, Pera J, Dziedzic T, Szczudlik A, Figlewicz DA.(2006)
DB-ID PON2_000001 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.26905 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     
PON2 NM_000305.2 ./. 8 c.932C>G r.(?) p.(Ser311Cys) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000378 ? ? PON2 1 Y Yang