Variant #0000341694 (NC_000023.10:g.153297719G>A, NM_004992.3:c.316C>T (MECP2))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153297719G>A
DNA change (hg38) g.154032268G>A
Published as MECP2(NM_004992.3):c.316C>T (p.R106W)
ISCN -
DB-ID MECP2_000165 See all 145 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MECP2 NM_001110792.1 +/. - c.352C>T r.(?) p.(Arg118Trp)
MECP2 NM_004992.3 +/. - c.316C>T r.(?) p.(Arg106Trp)


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