Variant #0000728202 (NC_000022.10:g.46733760A>T, NM_018006.4:c.167A>T (TRMU))

Chromosome 22
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.46733760A>T
DNA change (hg38) -
Published as TRMU(NM_018006.4):c.167A>T (p.D56V)
ISCN -
DB-ID GTSE1_000001
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTSE1 NM_016426.6 ?/. - c.*7733A>T r.(=) p.(=)
TRMU NM_018006.4 ?/. - c.167A>T r.(?) p.(Asp56Val)


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