Variant #0000289250 (NC_000002.11:g.74757647_74757649del, NM_032603.2:c.*3087_*3089del (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.74757647_74757649del
DNA change (hg38) g.74530520_74530522del
Published as HTRA2(NM_013247.4):c.506+8_506+10delTGG
ISCN -
DB-ID HTRA2_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) 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 2018-01-15 20:58:59 +01:00 (CET)
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.506+8_506+10del r.(=) p.(=)
LOXL3 NM_032603.2 ?/. - c.*3087_*3089del r.(=) p.(=)
DQX1 NM_133637.2 ?/. - c.-4403_-4401del r.(?) p.(=)
AUP1 NM_181575.3 ?/. - c.-890_-888del r.(?) p.(=)


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