Variant #0000574598 (NC_000023.10:g.153363117_153363119dup, NM_004992.3:c.-140_-138dup (MECP2))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.153363117_153363119dup
DNA change (hg38) g.154097660_154097662dup
Published as MECP2(NM_001110792.1):c.21_23dupCGC (p.A8dup), MECP2(NM_001110792.2):c.21_23dupCGC (p.A8dup)
ISCN -
DB-ID MECP2_002846 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.21_23dup r.(?) p.(Ala8dup)
MECP2 NM_004992.3 ?/. - c.-140_-138dup r.(?) p.(=)


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