Variant #0000807711 (NC_000016.9:g.89258859G>A, NC_000016.9(NM_004933.2):c.1855+7G>A (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.89258859G>A
DNA change (hg38) -
Published as CDH15(NM_004933.2):c.1855+7G>A
ISCN -
DB-ID CDH15_000052
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A31 NM_001242757.1 -?/. - c.*3548C>T r.(=) p.(=)
CDH15 NM_004933.2 -?/. - c.1855+7G>A r.(=) p.(=)


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