Variant #0000622642 (NC_000011.9:g.57558974G>C, NM_015959.3:c.*51257G>C (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.57558974G>C
DNA change (hg38) g.57791502G>C
Published as CTNND1(NM_001085458.1):c.24G>C (p.S8=)
ISCN -
DB-ID C11orf31_000015
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) 0.00031 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-30 16:36:37 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 -?/. - c.24G>C r.(?) p.(Ser8=)
BTBD18 NM_001145101.1 -?/. - c.-40010C>G r.(?) p.(=)
TMX2 NM_015959.3 -?/. - c.*51257G>C r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.*48670G>C r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.583G>C r.(?) -


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