Variant #0000693321 (NC_000023.10:g.124097495T>G, NM_014253.3:c.108A>C (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.124097495T>G
DNA change (hg38) -
Published as TENM1(NM_001163278.1):c.108A>C (p.P36=)
ISCN -
DB-ID ODZ1_000052
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 2020-09-15 15:50:26 +02:00 (CEST)
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.108A>C r.(?) p.(Pro36=)
ODZ1 NM_014253.3 -?/. - c.108A>C r.(?) p.(Pro36=)


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