Variant #0000544637 (NC_000011.9:g.57505852dup, NM_015959.3:c.391dup (TMX2))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57505852dup
DNA change (hg38) g.57738380dup
Published as TMX2(NM_015959.4):c.391dupC (p.L131Pfs*6)
ISCN -
DB-ID C11orf31_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
CTNND1 NM_001085458.1 +/. - c.-23953dup r.(?) p.(=)
BTBD18 NM_001145101.1 +/. - c.*5760dup r.(?) p.(=)
TMX2 NM_015959.3 +/. - c.391dup r.(?) p.(Leu131ProfsTer6)
C11orf31 NM_170746.2 +/. - c.-3216dup r.(?) p.(=)
TMX2-CTNND1 NR_037646.1 +/. - n.346+712dup r.(?) -


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