Variant #0000516995 (NC_000002.11:g.74777384C>T, NM_032603.2:c.405G>A (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.74777384C>T
DNA change (hg38) g.74550257C>T
Published as LOXL3(NM_032603.4):c.405G>A (p.T135=)
ISCN -
DB-ID DOK1_000002
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) 0.00229 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOK1 NM_001381.3 -?/. - c.-4498C>T r.(?) p.(=)
HTRA2 NM_013247.4 -?/. - c.*17272C>T r.(=) p.(=)
LOXL3 NM_032603.2 -?/. - c.405G>A r.(?) p.(Thr135=)


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