Variant #0001046318 (NC_000011.9:g.57573393_57573397del, NM_015959.3:c.*65676_*65680del (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.57573393_57573397del
DNA change (hg38) -
Published as CTNND1(NM_001085458.2):c.1762_1766delTATCA (p.Y588Sfs*38)
ISCN -
DB-ID C11orf31_000059
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 +/. - c.1762_1766del r.(?) p.(Tyr588Serfs*38)
BTBD18 NM_001145101.1 +/. - c.-54428_-54424del r.(?) p.(=)
TMX2 NM_015959.3 +/. - c.*65676_*65680del r.(=) p.(=)
C11orf31 NM_170746.2 +/. - c.*63089_*63093del r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 +/. - n.2321_2325del r.(?) -


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