Variant #0000329768 (NC_000003.11:g.195594864C>T, NM_005781.4:c.2260G>A (TNK2))

Chromosome 3
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.195594864C>T
DNA change (hg38) g.195867993C>T
Published as TNK2(NM_001010938.1):c.2494G>A (p.(Val832Ile)), TNK2(NM_005781.4):c.2260G>A (p.V754I)
ISCN -
DB-ID TNK2_000003 See all 2 reported entries
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) 3.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNK2 NM_005781.4 ?/. - c.2260G>A r.(?) p.(Val754Ile)


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