Variant #0000559805 (NC_000016.9:g.89260222G>T, NM_004933.2:c.2052G>T (CDH15))

Chromosome 16
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.89260222G>T
DNA change (hg38) g.89193814G>T
Published as CDH15(NM_004933.2):c.2052G>T (p.P684=)
ISCN -
DB-ID CDH15_000029
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-10 16:06:07 +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.*2185C>A r.(=) p.(=)
CDH15 NM_004933.2 -?/. - c.2052G>T r.(?) p.(Pro684=)


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