Variant #0000865700 (NC_000018.9:g.44118208C>A, NM_144612.6:c.4006G>T (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.44118208C>A
DNA change (hg38) -
Published as LOXHD1(NM_144612.6):c.4006G>T (p.V1336L)
ISCN -
DB-ID LOXHD1_000223
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) 0.00011 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LOXHD1 NM_001384474.1 ?/. - c.4006G>T r.(?) p.(Val1336Leu)
LOXHD1 NM_144612.6 ?/. - c.4006G>T r.(?) p.(Val1336Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.