Variant #0000559810 (NC_000016.9:g.89262685C>A, NM_004933.2:c.*1122C>A (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.89262685C>A
DNA change (hg38) g.89196277C>A
Published as SLC22A31(NM_001242757.1):c.739G>T (p.(Ala247Ser))
ISCN -
DB-ID CDH15_000034
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) 0.0004 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.739G>T r.(?) p.(Ala247Ser)
CDH15 NM_004933.2 ?/. - c.*1122C>A r.(=) p.(=)


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