Variant #0000658887 (NC_000022.10:g.21337303C>T, NC_000022.10(NM_006767.3):c.201-13C>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.21337303C>T
DNA change (hg38) g.20983014C>T
Published as LZTR1(NM_006767.4):c.201-13C>T
ISCN -
DB-ID AIFM3_000006
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) 0.00168 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LZTR1 NM_006767.3 -/. - c.201-13C>T r.(=) p.(=)
AIFM3 NM_144704.2 -/. - c.*1983C>T r.(=) p.(=)


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