Variant #0000004079 (NC_000023.10:g.153298014G>C, MECP2(NM_004992.3):c.27-6C>G)

Individual ID 00004079
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.153298014G>C
Reference Laccone F1, Huppke P, Hanefeld F, Meins M.(2001)
DB-ID MECP2_000205
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 ./. 1i c.27-6C>G r.(=) p.(=) VariO:0136 DNA substitution; VariO:0316 transversion -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004079 ? ? MECP2 1 Y Yang