Variant #0000975821 (NC_000003.11:g.42730366G>A, NM_152393.3:c.1427G>A (KLHL40))

Chromosome 3
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.42730366G>A
DNA change (hg38) -
Published as KLHL40(NM_152393.4):c.1427G>A (p.(Cys476Tyr))
ISCN -
DB-ID HHATL_000009
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) 1.0E-5 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     
HHATL NM_020707.3 ?/. - c.*3877C>T r.(=) p.(=)
KLHL40 NM_152393.3 ?/. - c.1427G>A r.(?) p.(Cys476Tyr)


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