Variant #0000255892 (NC_000011.9:g.57480254A>C, NM_015959.3:c.164A>C (TMX2))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57480254A>C
DNA change (hg38) g.57712782A>C
Published as TMX2(NM_015959.4):c.164A>C (p.D55A)
ISCN -
DB-ID TMX2_000002 See all 3 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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-49551A>C r.(?) p.(=)
BTBD18 NM_001145101.1 +/. - c.*31352T>G r.(=) p.(=)
TMX2 NM_015959.3 +/. - c.164A>C r.(?) p.(Asp55Ala)
MED19 NM_153450.1 +/. - c.-603T>G r.(?) p.(=)
C11orf31 NM_170746.2 +/. - c.-28814A>C r.(?) p.(=)
TMX2-CTNND1 NR_037646.1 +/. - n.260A>C r.(?) -


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