Variant #0001024824 (NC_000003.11:g.42733637G>T, NM_152393.3:c.*152G>T (KLHL40))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42733637G>T
DNA change (hg38) -
Published as KLHL40(NM_152393.4):c.*152G>T
ISCN -
DB-ID HHATL_000012 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +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     
HHATL NM_020707.3 +?/. - c.*606C>A r.(=) p.(=)
KLHL40 NM_152393.3 +?/. - c.*152G>T r.(=) p.(=)


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