Variant #0000278269 (NC_000001.10:g.112329551G>T, NC_000001.10(NM_004980.4):c.1269+15C>A (KCND3))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.112329551G>T
DNA change (hg38) g.111786929G>T
Published as KCND3(NM_004980.4):c.1269+15C>A, KCND3(NM_004980.5):c.1269+15C>A
ISCN -
DB-ID KCND3_000012 See all 2 reported entries
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) 0.16274 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCND3 NM_004980.4 -/. - c.1269+15C>A r.(=) p.(=)


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