Variant #0000676724 (NC_000002.11:g.74759957C>T, NM_032603.2:c.*776G>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.74759957C>T
DNA change (hg38) -
Published as HTRA2(NM_013247.4):c.1222C>T (p.R408W)
ISCN -
DB-ID AUP1_000007
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 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HTRA2 NM_013247.4 ?/. - c.1222C>T r.(?) p.(Arg408Trp)
LOXL3 NM_032603.2 ?/. - c.*776G>A r.(=) p.(=)
AUP1 NM_181575.3 ?/. - c.-3201G>A r.(?) p.(=)


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