Variant #0001038526 (NC_000011.9:g.57575754G>C, NM_015959.3:c.*68037G>C (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.57575754G>C
DNA change (hg38) -
Published as CTNND1(NM_001085458.2):c.2081G>C (p.(Gly694Ala))
ISCN -
DB-ID C11orf31_000056
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 2025-05-05 21:14:00 +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.2081G>C r.(?) p.(Gly694Ala)
BTBD18 NM_001145101.1 ?/. - c.-56790C>G r.(?) p.(=)
TMX2 NM_015959.3 ?/. - c.*68037G>C r.(=) p.(=)
C11orf31 NM_170746.2 ?/. - c.*65450G>C r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 ?/. - n.2640G>C r.(?) -


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