Variant #0000329359 (NC_000003.11:g.46751098_46751100del, NM_147196.2:c.391_393del (TMIE))

Chromosome 3
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.46751098_46751100del
DNA change (hg38) g.46709608_46709610del
Published as TMIE(NM_147196.2):c.370_372del (p.(Lys125del)), TMIE(NM_147196.2):c.391_393delAAG (p.K131del), TMIE(NM_147196.3):c.391_393delAAG (p.K131del)
ISCN -
DB-ID TMIE_000007
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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRSS50 NM_013270.4 ?/. - c.*2660_*2662del r.(=) p.(=)
TMIE NM_147196.2 ?/. - c.391_393del r.(?) p.(Lys131del)


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