Variant #0000657119 (NC_000012.11:g.5021347_5021348delinsAC, NM_000217.2:c.803_804delinsAC (KCNA1))

Chromosome 12
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.5021347_5021348delinsAC
DNA change (hg38) g.4912181_4912182delinsAC
Published as KCNA1(NM_000217.3):c.803_804delCGinsAC (p.T268N)
ISCN -
DB-ID KCNA1_000023
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNA1 NM_000217.2 ?/. - c.803_804delinsAC r.(?) p.(Thr268Asn)


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