Variant #0000003899 (NC_000023.10:g.103042790C>T, PLP1(NM_000533.3):c.517C>T)

Individual ID 00003899
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.103042790C>T
Reference Hübner CA1, Orth U, Senning A, Steglich C, Kohlschütter A, Korinthenberg R, Gal A.(2005)
DB-ID PLP1_000064 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
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.517C>T r.(?) p.(Pro173Ser) 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     
0000003899 ? ? PLP1 1 Y Yang