Variant #0000810737 (NC_000023.10:g.99662842G>A, NM_001184880.1:c.754C>T (PCDH19))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.99662842G>A
DNA change (hg38) -
Published as PCDH19(NM_001184880.1):c.754C>T (p.P252S), PCDH19(NM_001184880.2):c.754C>T (p.P252S)
ISCN -
DB-ID PCDH19_000238 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDH19 NM_001184880.1 ?/. - c.754C>T r.(?) p.(Pro252Ser)
PCDH19 NM_020766.2 ?/. - c.754C>T r.(?) p.(Pro252Ser)


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