Variant #0000285840 (NC_000003.11:g.42732481C>A, NM_152393.3:c.1738C>A (KLHL40))

Chromosome 3
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.42732481C>A
DNA change (hg38) g.42690989C>A
Published as KLHL40(NM_152393.4):c.1738C>A (p.L580I)
ISCN -
DB-ID KLHL40_000031
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) 0.00349 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HHATL NM_020707.3 -?/. - c.*1762G>T r.(=) p.(=)
KLHL40 NM_152393.3 -?/. - c.1738C>A r.(?) p.(Leu580Ile)


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