Variant #0001053913 (NC_000011.9:g.64060522dup, NM_033310.2:c.32dup (KCNK4))

Chromosome 11
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.64060522dup
DNA change (hg38) -
Published as KCNK4(NM_033310.3):c.32dup (p.(Leu12Alafs*56))
ISCN -
DB-ID BAD_000010
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 2025-11-01 13:22:20 +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     
GPR137 NM_020155.3 ?/. - c.*3685dup r.(?) p.(=)
BAD NM_032989.2 ?/. - c.-8428dup r.(?) p.(=)
KCNK4 NM_033310.2 ?/. - c.32dup r.(?) p.(Leu12Alafs*56)


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