Variant #0000889993 (NC_000011.9:g.57578974G>A, NM_015959.3:c.*71257G>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.57578974G>A
DNA change (hg38) -
Published as CTNND1(NM_001085458.2):c.2638+16G>A
ISCN -
DB-ID C11orf31_000034
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) 0.00039 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.2638+16G>A r.(=) p.(=)
BTBD18 NM_001145101.1 -?/. - c.-60010C>T r.(?) p.(=)
TMX2 NM_015959.3 -?/. - c.*71257G>A r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.*68670G>A r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.3197+16G>A r.(?) -


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