Variant #0000317972 (NC_000017.10:g.73512853C>T, NM_207346.2:c.83C>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.73512853C>T
DNA change (hg38) g.75516772C>T
Published as TSEN54(NM_207346.2):c.83C>T (p.S28L), TSEN54(NM_207346.3):c.83C>T (p.S28L)
ISCN -
DB-ID TSEN54_000003 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) 0.00112 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 ?/. - c.*17438C>T r.(=) p.(=)
CASKIN2 NM_020753.3 ?/. - c.-1776G>A r.(?) p.(=)
TSEN54 NM_207346.2 ?/. - c.83C>T r.(?) p.(Ser28Leu)


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