Variant #0000800818 (NC_000002.11:g.74274179dup, NM_144993.1:c.730dup (TET3))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74274179dup
DNA change (hg38) -
Published as TET3(NM_001287491.2):c.1135dupC (p.Q379Pfs*8)
ISCN -
DB-ID TET3_000023
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TET3 NM_001287491.1 +?/. - c.1135dup r.(?) p.(Gln379Profs*8)
TET3 NM_144993.1 +?/. - c.730dup r.(?) p.(Gln244Profs*8)


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