Variant #0000689085 (NC_000003.11:g.42730218G>A, NC_000003.11(NM_152393.3):c.1421+9G>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.42730218G>A
DNA change (hg38) -
Published as KLHL40(NM_152393.4):c.1421+9G>A
ISCN -
DB-ID HHATL_000006
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) 0.00039 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 2020-09-15 15:50:26 +02:00 (CEST)
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.*4025C>T r.(=) p.(=)
KLHL40 NM_152393.3 -?/. - c.1421+9G>A r.(=) p.(=)


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