Variant #0000616259 (NC_000016.9:g.89261352T>C, NM_004933.2:c.2234T>C (CDH15))

Chromosome 16
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.89261352T>C
DNA change (hg38) g.89194944T>C
Published as CDH15(NM_004933.2):c.2234T>C (p.V745A)
ISCN -
DB-ID CDH15_000038
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
SLC22A31 NM_001242757.1 ?/. - c.*1055A>G r.(=) p.(=)
CDH15 NM_004933.2 ?/. - c.2234T>C r.(?) p.(Val745Ala)


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