Variant #0001004535 (NC_000019.9:g.18778946_18778957dup, NM_018316.1:c.739_750dup (KLHL26))

Chromosome 19
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.18778946_18778957dup
DNA change (hg38) -
Published as KLHL26(NM_018316.1):c.739_750dupGTGCTCTGCCAC (p.(Val247_His250dup))
ISCN -
DB-ID KLHL26_000003
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLHL26 NM_018316.1 ?/. - c.739_750dup r.(?) p.(Val247_His250dup)


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