Variant #0001046705 (NC_000018.9:g.44171979C>T, NM_144612.6:c.1571G>A (LOXHD1))

Chromosome 18
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.44171979C>T
DNA change (hg38) -
Published as LOXHD1(NM_144612.7):c.1571G>A (p.R524H)
ISCN -
DB-ID LOXHD1_000171 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) 0.00042 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +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     
LOXHD1 NM_001384474.1 ?/. - c.1571G>A r.(?) p.(Arg524His)
LOXHD1 NM_144612.6 ?/. - c.1571G>A r.(?) p.(Arg524His)


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