Variant #0000003958 (NC_000023.10:g.153297959delG, MECP2(NM_004992.3):c.76delC)

Individual ID 00003958
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153297959delG
Reference Nielsen JB1, Henriksen KF, Hansen C, Silahtaroglu A, Schwartz M, Tommerup N.(2001)
DB-ID MECP2_000013
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 ./. 3 c.76delC r.(?) p.(Leu26Serfs*6) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000003958 ? ? MECP2 1 Y Yang