Variant #0000568179 (NC_000019.9:g.50824008G>A, NM_004977.2:c.2012C>T (KCNC3))

Chromosome 19
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.50824008G>A
DNA change (hg38) g.50320751G>A
Published as KCNC3(NM_004977.2):c.2012C>T (p.A671V), KCNC3(NM_004977.3):c.2012C>T (p.(Ala671Val))
ISCN -
DB-ID KCNC3_000032 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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNC3 NM_004977.2 ?/. - c.2012C>T r.(?) p.(Ala671Val)


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