Variant #0001033488 (NC_000002.11:g.74329187_74329190del, NM_144993.1:c.4867_4870del (TET3))

Chromosome 2
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.74329187_74329190del
DNA change (hg38) -
Published as TET3(NM_001287491.2):c.5272_5275del (p.(Glu1758Argfs*95))
ISCN -
DB-ID TET3_000060
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TET3 NM_001287491.1 ?/. - c.5272_5275del r.(?) p.(Glu1758Argfs*95)
TET3 NM_144993.1 ?/. - c.4867_4870del r.(?) p.(Glu1623Argfs*95)


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