Variant #0000896001 (NC_000023.10:g.153297759T>C, NM_004992.3:c.276A>G (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.153297759T>C
DNA change (hg38) -
Published as MECP2(NM_004992.4):c.276A>G (p.G92=)
ISCN -
DB-ID MECP2_002948
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) 6.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.312A>G r.(?) p.(Gly104=)
MECP2 NM_004992.3 -?/. - c.276A>G r.(?) p.(Gly92=)


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