Variant #0000856437 (NC_000023.10:g.153296824G>C, NM_004992.3:c.455C>G (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.153296824G>C
DNA change (hg38) -
Published as MECP2(NM_004992.3):c.455C>G (p.P152R)
ISCN -
DB-ID MECP2_000262 See all 73 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:47:41 +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.491C>G r.(?) p.(Pro164Arg)
MECP2 NM_004992.3 +/. - c.455C>G r.(?) p.(Pro152Arg)


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