Variant #0000003966 (NC_000023.10:g.153298007_153298008insCGGCG, MECP2(NM_004992.3):c.27_28insCGCCG)

Individual ID 00003966
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153298007_153298008insCGGCG
Reference Ravn K, Nielsen JB, Schwartz M.(2005)
DB-ID MECP2_000021
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 ./. 2 c.27_28insCGCCG r.(?) p.(Glu10Argfs*24) VariO:0142 DNA insertion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000003966 ? ? MECP2 1 Y Yang