Variant #0001006559 (NC_000023.10:g.153363117_153363119del, NM_004992.3:c.-140_-138del (MECP2))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153363117_153363119del
DNA change (hg38) -
Published as MECP2(NM_001110792.1):c.21_23delCGC (p.(Ala8del)), MECP2(NM_001110792.2):c.21_23delCGC (p.A8del)
ISCN -
DB-ID MECP2_002862 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.21_23del r.(?) p.(Ala8del)
MECP2 NM_004992.3 -?/. - c.-140_-138del r.(?) p.(=)


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