Variant #0000911784 (NC_000002.11:g.74763122C>T, NC_000002.11(NM_032603.2):c.1248+1G>A (LOXL3))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74763122C>T
DNA change (hg38) -
Published as LOXL3(NM_032603.5):c.1248+1G>A
ISCN -
DB-ID AUP1_000013
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +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     
HTRA2 NM_013247.4 +?/. - c.*3010C>T r.(=) p.(=)
LOXL3 NM_032603.2 +?/. - c.1248+1G>A r.spl? p.?
AUP1 NM_181575.3 +?/. - c.-6366G>A r.(?) p.(=)


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