Variant #0000524511 (NC_000005.9:g.140572950G>T, NM_019119.3:c.*3665G>T (PCDHB9))

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.140572950G>T
DNA change (hg38) g.141193377G>T
Published as PCDHB10(NM_018930.3):c.825G>T (p.A275=)
ISCN -
DB-ID PCDHB9_000004
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 17:13:04 +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.825G>T r.(?) p.(Ala275=)
PCDHB9 NM_019119.3 -?/. - c.*3665G>T r.(=) p.(=)


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