Variant #0000618967 (NC_000023.10:g.123518711G>A, NC_000023.10(NM_014253.3):c.6056-7C>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.123518711G>A
DNA change (hg38) g.124384861G>A
Published as TENM1(NM_001163278.1):c.6077-7C>T (p.(=))
ISCN -
DB-ID ODZ1_000041
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) 0.00085 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 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.6077-7C>T r.(=) p.(=)
ODZ1 NM_014253.3 -?/. - c.6056-7C>T r.(=) p.(=)


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