Variant #0000915416 (NC_000020.10:g.5935893A>G, NM_032485.5:c.482A>G (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.5935893A>G
DNA change (hg38) -
Published as MCM8(NM_001281520.1):c.482A>G (p.(His161Arg)), MCM8(NM_001281521.1):c.482A>G (p.H161R)
ISCN -
DB-ID MCM8_000003 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) 0.00105 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 2023-01-11 15:44:22 +01:00 (CET)
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.-4842T>C r.(?) p.(=)
MCM8 NM_032485.5 ?/. - c.482A>G r.(?) p.(His161Arg)


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