Variant #0000680964 (NC_000017.10:g.60651697_60651715del, NC_000017.10(NM_006852.3):c.1121+969_1121+987del (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.60651697_60651715del
DNA change (hg38) -
Published as TLK2(NM_001284333.1):c.1122-10_1130delTTTATGCTAGGCCCTCTTC, TLK2(NM_001284333.3):c.1122-10_1130delTTTATGCTAGGCCCTCTTC
ISCN -
DB-ID TLK2_000018 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLK2 NM_006852.3 ?/. - c.1121+969_1121+987del r.(=) p.(=)


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