Variant #0000999159 (NC_000011.9:g.57577619T>C, NM_015959.3:c.*69902T>C (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.57577619T>C
DNA change (hg38) -
Published as CTNND1(NM_001085458.1):c.2474T>C (p.V825A, p.(Val825Ala))
ISCN -
DB-ID TMX2-CTNND1_000007 See all 2 reported entries
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) 4.0E-5 View details
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.2474T>C r.(?) p.(Val825Ala)
BTBD18 NM_001145101.1 -?/. - c.-58655A>G r.(?) p.(=)
TMX2 NM_015959.3 -?/. - c.*69902T>C r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.*67315T>C r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.3033T>C r.(?) -


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