Variant #0000002569 (NC_000022.10:g.30070884G>A, NF2(NM_000268.3):c.1400G>A)

Individual ID 00002569
Chromosome 22
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.30070884G>A
Reference Yoo NJ1, Park SW, Lee SH.(2012)
DB-ID NF2_000086
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     
NF2 NM_000268.3 ./. 13 c.1400G>A r.(?) p.(Arg467Lys) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002569 ? ? NF2 1 Y Yang