Variant #0000719071 (NC_000002.11:g.74759825G>A, NM_032603.2:c.*908C>T (LOXL3))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74759825G>A
DNA change (hg38) -
Published as HTRA2(NM_013247.4):c.1195G>A (p.G399S), HTRA2(NM_013247.5):c.1195G>A (p.(Gly399Ser), p.G399S)
ISCN -
DB-ID HTRA2_000001 See all 5 reported entries
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) 0.00404 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HTRA2 NM_013247.4 -?/. - c.1195G>A r.(?) p.(Gly399Ser)
LOXL3 NM_032603.2 -?/. - c.*908C>T r.(=) p.(=)
AUP1 NM_181575.3 -?/. - c.-3069C>T r.(?) p.(=)


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