Variant #0000692431 (NC_000017.10:g.60655850A>T, NM_006852.3:c.1201A>T (TLK2))

Chromosome 17
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.60655850A>T
DNA change (hg38) -
Published as TLK2(NM_006852.3):c.1201A>T (p.(Ile401Phe)), TLK2(NM_006852.6):c.1201A>T (p.I401F)
ISCN -
DB-ID TLK2_000027 See all 3 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) 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLK2 NM_006852.3 ?/. - c.1201A>T r.(?) p.(Ile401Phe)


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