Variant #0000325618 (NC_000017.10:g.73518201A>T, NM_207346.2:c.1039A>T (TSEN54))

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.73518201A>T
DNA change (hg38) g.75522120A>T
Published as TSEN54(NM_207346.2):c.1039A>T (p.K347*, p.(Lys347*))
ISCN -
DB-ID TSEN54_000021 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) 4.0E-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 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LLGL2 NM_004524.2 ?/. - c.-3736A>T r.(?) p.(=)
TSEN54 NM_207346.2 ?/. - c.1039A>T r.(?) p.(Lys347Ter)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.