Variant #0001064637 (NC_000006.11:g.119150218T>A, NM_153255.4:c.*82571A>T (MCM9))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119150218T>A
DNA change (hg38) -
Published as MCM9(NM_017696.2):c.1521A>T (p.(Glu507Asp))
ISCN -
DB-ID ASF1A_000048
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) 0.00981 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 2026-01-20 18:57:21 +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     
ASF1A NM_014034.2 -/. - c.-65360T>A r.(?) p.(=)
MCM9 NM_153255.4 -/. - c.*82571A>T r.(=) p.(=)


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