Variant #0000895912 (NC_000023.10:g.123518206T>A, NM_014253.3:c.6554A>T (ODZ1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.123518206T>A
DNA change (hg38) -
Published as TENM1(NM_001163278.1):c.6575A>T (p.(His2192Leu))
ISCN -
DB-ID ODZ1_000025
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) 0.00577 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ODZ1 NM_001163278.1 -?/. - c.6575A>T r.(?) p.(His2192Leu)
ODZ1 NM_014253.3 -?/. - c.6554A>T r.(?) p.(His2185Leu)


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