Variant #0001043460 (NC_000020.10:g.5935329A>T, NM_032485.5:c.329A>T (MCM8))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.5935329A>T
DNA change (hg38) -
Published as MCM8(NM_032485.5):c.329A>T (p.Y110F), MCM8(NM_032485.6):c.329A>T (p.(Tyr110Phe))
ISCN -
DB-ID TRMT6_000002 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) 0.00268 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRMT6 NM_015939.3 -?/. - c.-4278T>A r.(?) p.(=)
MCM8 NM_032485.5 -?/. - c.329A>T r.(?) p.(Tyr110Phe)


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