Variant #0000003896 (NC_000023.10:g.103042754_103042755insGT, PLP1(NM_000533.3):c.481_482insGT)

Individual ID 00003896
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.103042754_103042755insGT
Reference Hübner CA1, Orth U, Senning A, Steglich C, Kohlschütter A, Korinthenberg R, Gal A.(2005)
DB-ID PLP1_000061
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     
PLP1 NM_000533.3 ./. 4 c.481_482insGT r.(?) p.(Val161Glyfs*38) VariO:0142 DNA insertion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000003896 ? ? PLP1 1 Y Yang