Variant #0000291662 (NC_000023.10:g.153297636G>C, NC_000023.10(NM_004992.3):c.377+22C>G (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.153297636G>C
DNA change (hg38) g.154032185G>C
Published as MECP2(NM_004992.3):c.377+22C>G
ISCN -
DB-ID MECP2_000147 See all 38 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) 0.02128 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.413+22C>G r.(=) p.(=)
MECP2 NM_004992.3 -/. - c.377+22C>G r.(=) p.(=)


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