Variant #0001064539 (NC_000006.11:g.39281850C>A, NC_000006.11(NM_031460.3):c.237+10G>T (KCNK17))

Chromosome 6
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.39281850C>A
DNA change (hg38) -
Published as KCNK17(NM_031460.4):c.237+10G>T
ISCN -
DB-ID KCNK16_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNK17 NM_031460.3 -?/. - c.237+10G>T r.(=) p.(=)
KCNK16 NM_032115.3 -?/. - c.*928G>T r.(=) p.(=)


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