Variant #0000577854 (NC_000023.10:g.99661952C>T, NM_001184880.1:c.1644G>A (PCDH19))

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.99661952C>T
DNA change (hg38) g.100406954C>T
Published as PCDH19(NM_001184880.2):c.1644G>A (p.T548=)
ISCN -
DB-ID PCDH19_000196
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) 8.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.1644G>A r.(?) p.(Thr548=)
PCDH19 NM_020766.2 -/. - c.1644G>A r.(?) p.(Thr548=)


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