Variant #0000524515 (NC_000005.9:g.140579737dup, NM_018930.3:c.*5209dup (PCDHB10))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140579737dup
DNA change (hg38) g.141200164dup
Published as PCDHB11(NM_018931.2):c.389_390insT (p.(Pro131SerfsTer51))
ISCN -
DB-ID PCDHB10_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 17:14:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHB10 NM_018930.3 -?/. - c.*5209dup r.(?) p.(=)
PCDHB11 NM_018931.2 -?/. - c.390dup r.(?) p.(Pro131SerfsTer51)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.