Variant #0000004135 (NC_000023.10:g.153296366_153296872delinsCTAAAAGC, MECP2(NM_004992.3):c.407_913delinsGCTTTTAG)

Individual ID 00004135
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153296366_153296872delinsCTAAAAGC
Reference Cheadle JP1, Gill H, Fleming N, Maynard J, Kerr A, Leonard H, Krawczak M, Cooper DN, Lynch S, Thomas N, Hughes H, Hulten M, Ravine D, Sampson JR, Clarke A.(2000)
DB-ID MECP2_000207
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     
MECP2 NM_004992.3 ./. 3 c.407_913delinsGCTTTTAG r.(?) p.(Val136Glyfs*3) VariO:0143 DNA indel VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004135 ? ? MECP2 1 Y Yang