Variant #0001016004 (NC_000023.10:g.153296472del, NM_004992.3:c.808del (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.153296472del
DNA change (hg38) -
Published as MECP2(NM_001369391.2):c.529delC (p.R177Efs*19)
ISCN -
DB-ID MECP2_000460 See all 20 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MECP2 NM_001110792.1 +/. - c.844del r.(?) p.(Arg282GlufsTer19)
MECP2 NM_004992.3 +/. - c.808del r.(?) p.(Arg270GlufsTer19)


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