Variant #0000977227 (NC_000006.11:g.39284597T>G, NM_031460.3:c.-2501A>C (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.39284597T>G
DNA change (hg38) -
Published as KCNK16(NM_001135106.2):c.622A>C (p.(Ile208Leu))
ISCN -
DB-ID KCNK16_000001
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) 0.00229 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.-2501A>C r.(?) p.(=)
KCNK16 NM_032115.3 -?/. - c.622A>C r.(?) p.(Ile208Leu)


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