Variant #0000618969 (NC_000023.10:g.123615651G>C, NM_014253.3:c.3859C>G (ODZ1))

Chromosome X
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.123615651G>C
DNA change (hg38) g.124481801G>C
Published as TENM1(NM_001163278.1):c.3880C>G (p.L1294V)
ISCN -
DB-ID ODZ1_000043
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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.3880C>G r.(?) p.(Leu1294Val)
ODZ1 NM_014253.3 ?/. - c.3859C>G r.(?) p.(Leu1287Val)


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