Variant #0001067285 (NC_000020.10:g.5933072C>T, NM_032485.5:c.151C>T (MCM8))

Chromosome 20
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.5933072C>T
DNA change (hg38) -
Published as MCM8(NM_001281521.1):c.151C>T (p.(Gln51Ter))
ISCN -
DB-ID TRMT6_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRMT6 NM_015939.3 ?/. - c.-2021G>A r.(?) p.(=)
MCM8 NM_032485.5 ?/. - c.151C>T r.(?) p.(Gln51*)


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