Variant #0000544636 (NC_000011.9:g.57480270C>G, NM_015959.3:c.180C>G (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.57480270C>G
DNA change (hg38) g.57712798C>G
Published as TMX2(NM_001347890.1):c.180C>G (p.D60E), TMX2(NM_015959.4):c.180C>G (p.D60E)
ISCN -
DB-ID C11orf31_000003 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) 0.00107 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNND1 NM_001085458.1 ?/. - c.-49535C>G r.(?) p.(=)
BTBD18 NM_001145101.1 ?/. - c.*31336G>C r.(=) p.(=)
TMX2 NM_015959.3 ?/. - c.180C>G r.(?) p.(Asp60Glu)
MED19 NM_153450.1 ?/. - c.-619G>C r.(?) p.(=)
C11orf31 NM_170746.2 ?/. - c.-28798C>G r.(?) p.(=)
TMX2-CTNND1 NR_037646.1 ?/. - n.276C>G r.(?) -


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