Variant #0000330590 (NC_000005.9:g.140558428C>G, NM_019120.3:c.813C>G (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.140558428C>G
DNA change (hg38) g.141178847C>G
Published as PCDHB8(NM_019120.3):c.813C>G (p.(Asp271Glu))
ISCN -
DB-ID PCDHB8_000001
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_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.*3630C>G r.(=) p.(=)
PCDHB8 NM_019120.3 ?/. - c.813C>G r.(?) p.(Asp271Glu)
PCDHB16 NM_020957.1 ?/. - c.-3707C>G r.(?) p.(=)


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