Variant #0000330592 (NC_000005.9:g.140559830G>C, NM_019120.3:c.2215G>C (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.140559830G>C
DNA change (hg38) g.141180249G>C
Published as PCDHB8(NM_019120.3):c.2215G>C (p.(Asp739His))
ISCN -
DB-ID PCDHB8_000003
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) 2.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHB7 NM_018940.2 ?/. - c.*5032G>C r.(=) p.(=)
PCDHB8 NM_019120.3 ?/. - c.2215G>C r.(?) p.(Asp739His)
PCDHB16 NM_020957.1 ?/. - c.-2305G>C r.(?) p.(=)


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