Variant #0000727150 (NC_000019.9:g.13226207C>T, NM_001136035.2:c.527G>A (TRMT1))

Chromosome 19
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.13226207C>T
DNA change (hg38) -
Published as TRMT1(NM_017722.5):c.527G>A (p.G176E)
ISCN -
DB-ID NACC1_000003
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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRMT1 NM_001136035.2 ?/. - c.527G>A r.(?) p.(Gly176Glu)
NACC1 NM_052876.3 ?/. - c.-3070C>T r.(?) p.(=)


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