Variant #0000984127 (NC_000022.10:g.21351090G>T, NM_006767.3:c.2325G>T (LZTR1))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21351090G>T
DNA change (hg38) -
Published as LZTR1(NM_006767.3):c.2325G>T (p.Q775H), LZTR1(NM_006767.4):c.2325G>T (p.(Gln775His), p.Q775H)
ISCN -
DB-ID LZTR1_000087 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 2024-04-19 20:27:30 +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.2325G>T r.(?) p.(Gln775His)
THAP7 NM_030573.2 +?/. - c.*3079C>A r.(=) p.(=)


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