Variant #0000326384 (NC_000019.9:g.36394267del, NM_003332.3:c.*1204del (TYROBP))

Chromosome 19
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.36394267del
DNA change (hg38) g.35903365del
Published as HCST(NM_001007469.1):c.58del (p.(Thr20ArgfsTer84))
ISCN -
DB-ID HCST_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 17:24:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYROBP NM_003332.3 ?/. - c.*1204del r.(?) p.(=)
HCST NM_014266.3 ?/. - c.58del r.(?) p.(Thr20ArgfsTer85)
NFKBID NM_139239.1 ?/. - c.-3289del r.(?) p.(=)


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