Variant #0000896392 (NC_000023.10:g.99662015C>G, NM_001184880.1:c.1581G>C (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.99662015C>G
DNA change (hg38) -
Published as PCDH19(NM_001184880.1):c.1581G>C (p.K527N)
ISCN -
DB-ID PCDH19_000246
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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDH19 NM_001184880.1 ?/. - c.1581G>C r.(?) p.(Lys527Asn)
PCDH19 NM_020766.2 ?/. - c.1581G>C r.(?) p.(Lys527Asn)


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