Variant #0000521189 (NC_000004.11:g.110791657_110791659del, NM_198506.4:c.1752_1754del (LRIT3))

Chromosome 4
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.110791657_110791659del
DNA change (hg38) g.109870501_109870503del
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

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


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