Variant #0000544644 (NC_000011.9:g.57573960_57573961insA, NM_015959.3:c.*66243_*66244insA (TMX2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57573960_57573961insA
DNA change (hg38) g.57806488_57806489insA
Published as CTNND1(NM_001085458.1):c.1894+10_1894+11insA
ISCN -
DB-ID C11orf31_000011
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 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 -?/. - c.1894+10_1894+11insA r.(=) p.(=)
BTBD18 NM_001145101.1 -?/. - c.-54997_-54996insT r.(?) p.(=)
TMX2 NM_015959.3 -?/. - c.*66243_*66244insA r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.*63656_*63657insA r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.2453+10_2453+11insA r.(?) -


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