Variant #0000999153 (NC_000011.9:g.57564292C>T, NM_015959.3:c.*56575C>T (TMX2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57564292C>T
DNA change (hg38) -
Published as CTNND1(NM_001085458.1):c.784C>T (p.(Gln262*))
ISCN -
DB-ID C11orf31_000046
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.784C>T r.(?) p.(Gln262*)
BTBD18 NM_001145101.1 +?/. - c.-45328G>A r.(?) p.(=)
TMX2 NM_015959.3 +?/. - c.*56575C>T r.(=) p.(=)
C11orf31 NM_170746.2 +?/. - c.*53988C>T r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 +?/. - n.1343C>T r.(?) -


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