Variant #0000618245 (NC_000020.10:g.5935823A>G, NM_032485.5:c.412A>G (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.5935823A>G
DNA change (hg38) g.5955177A>G
Published as MCM8(NM_001281521.1):c.412A>G (p.I138V)
ISCN -
DB-ID MCM8_000002
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRMT6 NM_015939.3 -?/. - c.-4772T>C r.(?) p.(=)
MCM8 NM_032485.5 -?/. - c.412A>G r.(?) p.(Ile138Val)


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