Variant #0000269905 (NC_000016.9:g.89261482C>A, NM_004933.2:c.2364C>A (CDH15))

Chromosome 16
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.89261482C>A
DNA change (hg38) g.89195074C>A
Published as CDH15(NM_004933.3):c.2364C>A (p.Y788*)
ISCN -
DB-ID CDH15_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) 0.06533 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A31 NM_001242757.1 -/. - c.*925G>T r.(=) p.(=)
CDH15 NM_004933.2 -/. - c.2364C>A r.(?) p.(Tyr788Ter)


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