Variant #0000804640 (NC_000010.10:g.95549850_95549851dup, NC_000010.10(NM_005097.2):c.432-6_432-5dup (LGI1))

Chromosome 10
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.95549850_95549851dup
DNA change (hg38) -
Published as LGI1(NM_005097.3):c.432-6_432-5dupTT, LGI1(NM_005097.4):c.432-6_432-5dupTT
ISCN -
DB-ID LGI1_000008 See all 2 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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     
LGI1 NM_005097.2 -?/. - c.432-6_432-5dup r.spl? p.?


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