Variant #0000534631 (NC_000008.10:g.27293270_27293271del, NM_004103.4:c.1203_1204del (PTK2B))

Chromosome 8
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.27293270_27293271del
DNA change (hg38) g.27435753_27435754del
Published as PTK2B(NM_004103.4):c.1202_1203del (p.(Tyr402ArgfsTer21))
ISCN -
DB-ID PTK2B_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 18:14:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTK2B NM_004103.4 ?/. - c.1203_1204del r.(?) p.(Tyr402ArgfsTer21)


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