Variant #0001051811 (NC_000004.11:g.110791657_110791659del, NM_198506.4:c.1752_1754del (LRIT3))

Chromosome 4
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.110791657_110791659del
DNA change (hg38) -
Published as LRIT3(NM_198506.4):c.1752_1754delTCT (p.L585del), LRIT3(NM_198506.5):c.1752_1754del (p.(Leu585del)), LRIT3(NM_198506.5):c.1752_1754delTCT (p.L585del)
ISCN -
DB-ID LRIT3_000031 See all 3 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRIT3 NM_198506.4 ?/. - c.1752_1754del r.(?) p.(Leu585del)


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