Variant #0000330605 (NC_000005.9:g.140595302A>G, NM_018932.3:c.*4435A>G (PCDHB12))

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.140595302A>G
DNA change (hg38) g.141215730A>G
Published as PCDHB13(NM_018933.3):c.1607A>G (p.(His536Arg))
ISCN -
DB-ID PCDHB13_000008
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) 0.00383 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     
PCDHB12 NM_018932.3 ?/. - c.*4435A>G r.(=) p.(=)
PCDHB13 NM_018933.2 ?/. - c.1607A>G r.(?) p.(His536Arg)


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