Variant #0000853037 (NC_000011.9:g.57578943C>T, NM_015959.3:c.*71226C>T (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.57578943C>T
DNA change (hg38) -
Published as CTNND1(NM_001085458.1):c.2623C>T (p.R875W), CTNND1(NM_001085458.2):c.2623C>T (p.R875W)
ISCN -
DB-ID C11orf31_000032 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) 0.00069 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 -?/. - c.2623C>T r.(?) p.(Arg875Trp)
BTBD18 NM_001145101.1 -?/. - c.-59979G>A r.(?) p.(=)
TMX2 NM_015959.3 -?/. - c.*71226C>T r.(=) p.(=)
C11orf31 NM_170746.2 -?/. - c.*68639C>T r.(=) p.(=)
TMX2-CTNND1 NR_037646.1 -?/. - n.3182C>T r.(?) -


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