Variant #0000340888 (NC_000022.10:g.21351018C>T, NM_006767.3:c.2253C>T (LZTR1))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21351018C>T
DNA change (hg38) g.20996729C>T
Published as LZTR1(NM_006767.3):c.2253C>T (p.F751=), LZTR1(NM_006767.4):c.2253C>T (p.F751=, p.(Phe751=))
ISCN -
DB-ID LZTR1_000086 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) 0.01582 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LZTR1 NM_006767.3 -/. - c.2253C>T r.(?) p.(Phe751=)
THAP7 NM_030573.2 -/. - c.*3151G>A r.(=) p.(=)


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