Variant #0000720221 (NC_000005.9:g.140480367T>A, NM_018936.2:c.*3596T>A (PCDHB2))

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.140480367T>A
DNA change (hg38) -
Published as PCDHB3(NM_018937.4):c.134T>A (p.I45K)
ISCN -
DB-ID PCDHB2_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHB2 NM_018936.2 ?/. - c.*3596T>A r.(=) p.(=)
PCDHB3 NM_018937.2 ?/. - c.134T>A r.(?) p.(Ile45Lys)


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