Variant #0000330593 (NC_000005.9:g.140569161dup, NM_019119.3:c.2270dup (PCDHB9))

Chromosome 5
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.140569161dup
DNA change (hg38) g.141189588dup
Published as PCDHB9(NM_019119.3):c.2267_2268insG (p.(Glu757GlyfsTer?))
ISCN -
DB-ID PCDHB9_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHB10 NM_018930.3 ?/. - c.-2965dup r.(?) p.(=)
PCDHB9 NM_019119.3 ?/. - c.2270dup r.(?) p.(Gly758ArgfsTer21)
PCDHB16 NM_020957.1 ?/. - c.*4696dup r.(?) p.(=)


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