Variant #0000004279 (NC_000023.10:g.153296882G>A, MECP2(NM_004992.3):c.397C>T)

Individual ID 00004279
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153296882G>A
Reference Neul JL1, Lane JB2, Lee HS3, Geerts S2, Barrish JO4, Annese F5, Baggett LM5, Barnes K6, Skinner SA5, Motil KJ4, Glaze DG4, Kaufmann WE6, Percy AK2.(2014)
DB-ID MECP2_000001 See all 9 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
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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 ./. 4 c.397C>T r.(?) p.(Arg133Cys) 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     
0000004279 ? ? MECP2 1 Y Yang