Variant #0000853033 (NC_000011.9:g.57492041C>T, NC_000011.9(NM_015959.3):c.189+11762C>T (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.57492041C>T
DNA change (hg38) -
Published as TMX2(NM_001347891.1):c.196C>T (p.R66C), TMX2(NM_001347891.2):c.196C>T (p.(Arg66Cys))
ISCN -
DB-ID C11orf31_000027 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_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 2024-04-19 20:27:30 +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.-37764C>T r.(?) p.(=)
BTBD18 NM_001145101.1 ?/. - c.*19565G>A r.(=) p.(=)
TMX2 NM_015959.3 ?/. - c.189+11762C>T r.(=) p.(=)
C11orf31 NM_170746.2 ?/. - c.-17027C>T r.(?) p.(=)
TMX2-CTNND1 NR_037646.1 ?/. - n.285+11762C>T r.(?) -


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