Variant #0000003926 (NC_000023.10:g.103042740C>T, PLP1(NM_000533.3):c.467C>T)

Individual ID 00003926
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.103042740C>T
Reference Xie H1, Feng H2, Ji J3, Wu Y1, Kou L3, Li D1, Ji H1, Wu X1, Niu Z4, Wang J5, Jiang Y6.(2014)
DB-ID PLP1_000008 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
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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.467C>T r.(?) p.(Thr156Ile) 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     
0000003926 ? ? PLP1 1 Y Yang