Variant #0000524527 (NC_000005.9:g.140590728A>G, NM_018932.3:c.2249A>G (PCDHB12))

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.140590728A>G
DNA change (hg38) g.141211156A>G
Published as PCDHB12(NM_018932.3):c.2249A>G (p.(His750Arg))
ISCN -
DB-ID PCDHB12_000015
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) 0.00065 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 2019-07-18 18:22:55 +02:00 (CEST)
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.2249A>G r.(?) p.(His750Arg)
PCDHB13 NM_018933.2 -?/. - c.-2968A>G r.(?) p.(=)


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