Variant #0000296795 (NC_000023.10:g.99662756G>C, NM_001184880.1:c.840C>G (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.99662756G>C
DNA change (hg38) g.100407758G>C
Published as PCDH19(NM_001184880.2):c.840C>G (p.Y280*)
ISCN -
DB-ID PCDH19_000064 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.840C>G r.(?) p.(Tyr280Ter)
PCDH19 NM_020766.2 +/. - c.840C>G r.(?) p.(Tyr280Ter)


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