Variant #0000994008 (NC_000004.11:g.110791682_110791683del, NM_198506.4:c.1777_1778del (LRIT3))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110791682_110791683del
DNA change (hg38) -
Published as LRIT3(NM_198506.5):c.1777_1778delGT (p.V593Cfs*19)
ISCN -
DB-ID LRIT3_000046
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRIT3 NM_198506.4 +?/. - c.1777_1778del r.(?) p.(Val593Cysfs*19)


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