Variant #0001006558 (NC_000023.10:g.153363090_153363092dup, NM_004992.3:c.-116_-114dup (MECP2))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153363090_153363092dup
DNA change (hg38) -
Published as MECP2(NM_001110792.2):c.45_47dup (p.(Gly16dup)), MECP2(NM_004992.3):c.-116_-114dupAGG
ISCN -
DB-ID MECP2_000241 See all 15 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.45_47dup r.(?) p.(Gly16dup)
MECP2 NM_004992.3 -/. - c.-116_-114dup r.(?) p.(=)


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