Variant #0000654719 (NC_000002.11:g.74328963G>A, NM_144993.1:c.4643G>A (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.74328963G>A
DNA change (hg38) g.74101836G>A
Published as TET3(NM_001287491.2):c.5048G>A (p.R1683H)
ISCN -
DB-ID TET3_000018
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +01:00 (CET)
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.5048G>A r.(?) p.(Arg1683His)
TET3 NM_144993.1 ?/. - c.4643G>A r.(?) p.(Arg1548His)


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