Variant #0001005924 (NC_000022.10:g.21340186G>C, NM_006767.3:c.320G>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.21340186G>C
DNA change (hg38) -
Published as LZTR1(NM_006767.3):c.320G>C (p.R107T, p.(Arg107Thr))
ISCN -
DB-ID LZTR1_000061 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 2024-08-28 13:16:32 +02:00 (CEST)
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.320G>C r.(?) p.(Arg107Thr)
AIFM3 NM_144704.2 ?/. - c.*4866G>C r.(=) p.(=)


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