Variant #0000729269 (NC_000023.10:g.99662720del, NM_001184880.1:c.878del (PCDH19))

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.99662720del
DNA change (hg38) -
Published as PCDH19(NM_001184880.2):c.878delC (p.P293Rfs*12)
ISCN -
DB-ID PCDH19_000225
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDH19 NM_001184880.1 +/. - c.878del r.(?) p.(Pro293Argfs*12)
PCDH19 NM_020766.2 +/. - c.878del r.(?) p.(Pro293Argfs*12)


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