Variant #0000574533 (NC_000023.10:g.153295944C>T, NM_004992.3:c.1335G>A (MECP2))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153295944C>T
DNA change (hg38) g.154030493C>T
Published as MECP2(NM_004992.3):c.1335G>A (p.T445=)
ISCN -
DB-ID MECP2_000240 See all 12 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) 0.00129 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.1371G>A r.(?) p.(Thr457=)
MECP2 NM_004992.3 -/. - c.1335G>A r.(?) p.(Thr445=)


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