Variant #0000608974 (NC_000004.11:g.110772820G>A, NM_198506.4:c.277G>A (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.110772820G>A
DNA change (hg38) g.109851664G>A
Published as LRIT3(NM_198506.4):c.277G>A (p.V93M), LRIT3(NM_198506.5):c.277G>A (p.V93M)
ISCN -
DB-ID LRIT3_000003 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) 4.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.277G>A r.(?) p.(Val93Met)


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