Variant #0000618488 (NC_000022.10:g.21350272G>A, NM_006767.3:c.2090G>A (LZTR1))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21350272G>A
DNA change (hg38) g.20995983G>A
Published as LZTR1(NM_006767.3):c.2090G>A (p.(Arg697Gln)), LZTR1(NM_006767.4):c.2090G>A (p.R697Q)
ISCN -
DB-ID LZTR1_000122 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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LZTR1 NM_006767.3 ?/. - c.2090G>A r.(?) p.(Arg697Gln)
THAP7 NM_030573.2 ?/. - c.*3897C>T r.(=) p.(=)


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