Variant #0000692205 (NC_000016.9:g.89261277A>C, NM_004933.2:c.2159A>C (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.89261277A>C
DNA change (hg38) -
Published as CDH15(NM_004933.3):c.2159A>C (p.E720A)
ISCN -
DB-ID CDH15_000045
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) 0.00011 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.*1130T>G r.(=) p.(=)
CDH15 NM_004933.2 -?/. - c.2159A>C r.(?) p.(Glu720Ala)


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