Variant #0001013787 (NC_000002.11:g.74777472C>A, NM_032603.2:c.317G>T (LOXL3))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74777472C>A
DNA change (hg38) -
Published as LOXL3(NM_032603.5):c.317G>T (p.R106L)
ISCN -
DB-ID DOK1_000005
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) 0.00527 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOK1 NM_001381.3 -/. - c.-4410C>A r.(?) p.(=)
HTRA2 NM_013247.4 -/. - c.*17360C>A r.(=) p.(=)
LOXL3 NM_032603.2 -/. - c.317G>T r.(?) p.(Arg106Leu)


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