Variant #0000895604 (NC_000022.10:g.21351236T>C, NM_006767.3:c.2387T>C (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.21351236T>C
DNA change (hg38) -
Published as LZTR1(NM_006767.4):c.2387T>C (p.(Ile796Thr), p.I796T)
ISCN -
DB-ID LZTR1_000201 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) 7.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LZTR1 NM_006767.3 ?/. - c.2387T>C r.(?) p.(Ile796Thr)
THAP7 NM_030573.2 ?/. - c.*2933A>G r.(=) p.(=)


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