Variant #0000000028 (NC_000010.10:g.55700727G>A, PCDH15(NM_001142772.1):c.3131C>T)

Individual ID 00000036
Chromosome 10
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.55700727G>A
Reference -
DB-ID PCDH15_000001
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
PCDH15 NM_001142772.1 +?/+? - c.3131C>T r.(?) p.(Pro1044Leu) VUS LP



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000037 DNA SEQ-NG PCDH15 1 variome.ir