Variant #0000344693 (NC_000017.10:g.44248783G>T, NM_001193466.1:c.727C>A (KANSL1))

Chromosome 17
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.44248783G>T
DNA change (hg38) g.46171417G>T
Published as KANSL1(NM_001193466.1):c.727C>A (p.Q243K), KANSL1(NM_001193466.2):c.727C>A (p.Q243K)
ISCN -
DB-ID KANSL1_000067 See all 3 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) 0.00183 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KANSL1 NM_001193466.1 -/. - c.727C>A r.(?) p.(Gln243Lys)


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