Variant #0000502498 (NC_000001.10:g.112525344G>T, NM_004980.4:c.5C>A (KCND3))

Chromosome 1
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.112525344G>T
DNA change (hg38) g.111982722G>T
Published as KCND3(NM_001378969.1):c.5C>A (p.(Ala2Glu)), KCND3(NM_004980.4):c.5C>A (p.A2E), KCND3(NM_004980.5):c.5C>A (p.A2E)
ISCN -
DB-ID KCND3_000049 See all 5 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) 0.00051 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCND3 NM_004980.4 -?/. - c.5C>A r.(?) p.(Ala2Glu)


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