Variant #0000568190 (NC_000019.9:g.50831705_50831713dup, NM_004977.2:c.642_650dup (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.50831705_50831713dup
DNA change (hg38) g.50328448_50328456dup
Published as KCNC3(NM_004977.2):c.642_650dupCAACGCCGC (p.N215_A217dup)
ISCN -
DB-ID KCNC3_000037
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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNC3 NM_004977.2 ?/. - c.642_650dup r.(?) p.(Asn215_Ala217dup)


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