Variant #0001043740 (NC_000022.10:g.21350074G>A, NM_006767.3:c.1982G>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.21350074G>A
DNA change (hg38) -
Published as LZTR1(NM_006767.3):c.1982G>A (p.G661E), LZTR1(NM_006767.4):c.1982G>A (p.G661E, p.(Gly661Glu))
ISCN -
DB-ID LZTR1_000121 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LZTR1 NM_006767.3 ?/. - c.1982G>A r.(?) p.(Gly661Glu)
THAP7 NM_030573.2 ?/. - c.*4095C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.