Variant #0000855310 (NC_000018.9:g.44152119C>T, NM_144612.6:c.1977G>A (LOXHD1))

Chromosome 18
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.44152119C>T
DNA change (hg38) -
Published as LOXHD1(NM_144612.6):c.1977G>A (p.L659=)
ISCN -
DB-ID LOXHD1_000225
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.1977G>A r.(?) p.(Leu659=)
LOXHD1 NM_144612.6 -?/. - c.1977G>A r.(?) p.(Leu659=)


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