Variant #0000999148 (NC_000011.9:g.57506506_57506526del, NC_000011.9(NM_015959.3):c.609_614+15del (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.57506506_57506526del
DNA change (hg38) -
Published as TMX2(NM_015959.3):c.609_614+15delTACGCGGTATGTAAAGACCTG (p.(Ser203_Thr204del))
ISCN -
DB-ID TMX2_000010 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) 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.-23299_-23279del r.(?) p.(=)
BTBD18 NM_001145101.1 ?/. - c.*5081_*5101del r.(=) p.(=)
TMX2 NM_015959.3 ?/. - c.609_614+15del r.spl? p.?
C11orf31 NM_170746.2 ?/. - c.-2562_-2542del r.(?) p.(=)
TMX2-CTNND1 NR_037646.1 ?/. - n.346+1366_346+1386del r.(?) -


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