Variant #0000286205 (NC_000023.10:g.153296689G>A, NM_004992.3:c.590C>T (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.153296689G>A
DNA change (hg38) g.154031238G>A
Published as MECP2(NM_001110792.1):c.626C>T (p.(Thr209Met)), MECP2(NM_004992.3):c.590C>T (p.T197M)
ISCN -
DB-ID MECP2_000528 See all 23 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) 0.00064 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MECP2 NM_001110792.1 -?/. - c.626C>T r.(?) p.(Thr209Met)
MECP2 NM_004992.3 -?/. - c.590C>T r.(?) p.(Thr197Met)


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