Variant #0000976598 (NC_000005.9:g.140201785_140201786del, NC_000005.9(NM_018900.2):c.2394+33516_2394+33517del (PCDHA1))

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.140201785_140201786del
DNA change (hg38) -
Published as PCDHA5(NM_018908.3):c.425_426del (p.(Leu142*))
ISCN -
DB-ID PCDHA1_000064
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHAC1 NM_018898.3 ?/. - c.-104693_-104692del r.(?) p.(=)
PCDHAC2 NM_018899.5 ?/. - c.-144567_-144566del r.(?) p.(=)
PCDHA1 NM_018900.2 ?/. - c.2394+33516_2394+33517del r.(=) p.(=)
PCDHA10 NM_018901.2 ?/. - c.-33849_-33848del r.(?) p.(=)
PCDHA11 NM_018902.3 ?/. - c.-46904_-46903del r.(?) p.(=)
PCDHA12 NM_018903.2 ?/. - c.-53273_-53272del r.(?) p.(=)
PCDHA13 NM_018904.2 ?/. - c.-60069_-60068del r.(?) p.(=)
PCDHA2 NM_018905.2 ?/. - c.2388+24848_2388+24849del r.(=) p.(=)
PCDHA3 NM_018906.2 ?/. - c.2394+18609_2394+18610del r.(=) p.(=)
PCDHA4 NM_018907.2 ?/. - c.2385+12628_2385+12629del r.(=) p.(=)
PCDHA5 NM_018908.2 ?/. - c.425_426del r.(?) p.(Leu142*)
PCDHA6 NM_018909.2 ?/. - c.-5892_-5891del r.(?) p.(=)
PCDHA7 NM_018910.2 ?/. - c.-12184_-12183del r.(?) p.(=)
PCDHA8 NM_018911.2 ?/. - c.-19122_-19121del r.(?) p.(=)
PCDHA9 NM_031857.1 ?/. - c.-26296_-26295del r.(?) p.(=)


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