Variant #0000004082 (NC_000023.10:g.153296840delC, MECP2(NM_004992.3):c.439delG)

Individual ID 00004082
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153296840delC
Reference Bourdon V1, Philippe C, Labrune O, Amsallem D, Arnould C, Jonveaux P.(2001)
DB-ID MECP2_000130
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     
MECP2 NM_004992.3 ./. 4 c.439delG r.(?) p.(Asp147Thrfs*13) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004082 ? ? MECP2 1 Y Yang