Variant #0000613459 (NC_000011.9:g.57571096C>T, NM_015959.3:c.*63379C>T (TMX2))

Chromosome 11
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.57571096C>T
DNA change (hg38) g.57803624C>T
Published as CTNND1(NM_001085458.1):c.1424C>T (p.T475I)
ISCN -
DB-ID C11orf31_000017
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) 1.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-30 16:39:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 ?/. - c.1424C>T r.(?) p.(Thr475Ile)
BTBD18 NM_001145101.1 ?/. - c.-52132G>A r.(?) p.(=)
TMX2 NM_015959.3 ?/. - c.*63379C>T r.(=) p.(=)
C11orf31 NM_170746.2 ?/. - c.*60792C>T r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 ?/. - n.1983C>T r.(?) -


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