Variant #0000325616 (NC_000017.10:g.73512644_73512649dup, NM_207346.2:c.3_8dup (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.73512644_73512649dup
DNA change (hg38) g.75516563_75516568dup
Published as TSEN54(NM_207346.2):c.2_3insGGAGCC (p.(Met1_Glu2insGluPro)), TSEN54(NM_207346.2):c.3_8dupGGAGCC (p.E6_P7dup), TSEN54(NM_207346.3):c.3_8dupGGAGCC ...)
ISCN -
DB-ID TSEN54_000001 See all 3 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_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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 ?/. - c.*17229_*17234dup r.(=) p.(=)
CASKIN2 NM_020753.3 ?/. - c.-1572_-1567dup r.(?) p.(=)
TSEN54 NM_207346.2 ?/. - c.3_8dup r.(?) p.(Met1?)


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