Variant #0000330591 (NC_000005.9:g.140559334C>A, NM_019120.3:c.1719C>A (PCDHB8))

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.140559334C>A
DNA change (hg38) g.141179753C>A
Published as PCDHB8(NM_019120.3):c.1719C>A (p.(Cys573Ter))
ISCN -
DB-ID PCDHB8_000002
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) 0.00111 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-17 17:09:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHB7 NM_018940.2 ?/. - c.*4536C>A r.(=) p.(=)
PCDHB8 NM_019120.3 ?/. - c.1719C>A r.(?) p.(Cys573Ter)
PCDHB16 NM_020957.1 ?/. - c.-2801C>A r.(?) p.(=)


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