Variant #0000516994 (NC_000002.11:g.74760062C>T, NM_032603.2:c.*671G>A (LOXL3))

Chromosome 2
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.74760062C>T
DNA change (hg38) g.74532935C>T
Published as HTRA2(NM_013247.4):c.1327C>T (p.(Arg443Trp))
ISCN -
DB-ID AUP1_000004
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HTRA2 NM_013247.4 ?/. - c.1327C>T r.(?) p.(Arg443Trp)
LOXL3 NM_032603.2 ?/. - c.*671G>A r.(=) p.(=)
AUP1 NM_181575.3 ?/. - c.-3306G>A r.(?) p.(=)


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