Variant #0000723504 (NC_000011.9:g.57582878C>A, NM_015959.3:c.*75161C>A (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.57582878C>A
DNA change (hg38) -
Published as CTNND1(NM_001085458.1):c.2714C>A (p.S905Y)
ISCN -
DB-ID C11orf31_000025
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) 0.00034 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 -?/. - c.2714C>A r.(?) p.(Ser905Tyr)
BTBD18 NM_001145101.1 -?/. - c.-63914G>T r.(?) p.(=)
TMX2 NM_015959.3 -?/. - c.*75161C>A r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.*72574C>A r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.3273C>A r.(?) -


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