Variant #0000928657 (NC_000002.11:g.74275412C>G, NM_144993.1:c.1963C>G (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.74275412C>G
DNA change (hg38) -
Published as TET3(NM_001287491.2):c.2368C>G (p.P790A)
ISCN -
DB-ID TET3_000037
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TET3 NM_001287491.1 ?/. - c.2368C>G r.(?) p.(Pro790Ala)
TET3 NM_144993.1 ?/. - c.1963C>G r.(?) p.(Pro655Ala)


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