Variant #0001057079 (NC_000022.10:g.21336687dup, NM_006767.3:c.27dup (LZTR1))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21336687dup
DNA change (hg38) -
Published as LZTR1(NM_006767.4):c.27dup (p.(Gln10AlafsTer24))
ISCN -
DB-ID AIFM3_000013
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LZTR1 NM_006767.3 +/. - c.27dup r.(?) p.(Gln10Alafs*24)
AIFM3 NM_144704.2 +/. - c.*1367dup r.(?) p.(=)


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