Variant #0000656500 (NC_000010.10:g.55581936G>T, NM_033056.3:c.5550C>A (PCDH15))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55581936G>T
DNA change (hg38) g.53822176G>T
Published as PCDH15(NM_001142763.1):c.5571C>A (p.T1857=), PCDH15(NM_033056.4):c.5550C>A (p.T1850=)
ISCN -
DB-ID PCDH15_000148 See all 3 reported entries
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) 0.00104 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDH15 NM_033056.3 -/. - c.5550C>A r.(?) p.(Thr1850=)


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