Variant #0000003947 (NC_000023.10:g.153296815A>G, MECP2(NM_004992.3):c.464T>C)

Individual ID 00003947
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153296815A>G
Reference Amir RE1, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY.(1999)
DB-ID MECP2_000002
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.464T>C r.(?) p.(Phe155Ser) 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     
0000003947 ? ? MECP2 1 Y Yang