Variant #0000887025 (NC_000006.11:g.119252737T>A, NM_153255.4:c.152A>T (MCM9))

Chromosome 6
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.119252737T>A
DNA change (hg38) -
Published as MCM9(NM_017696.3):c.152A>T (p.N51I)
ISCN -
DB-ID ASF1A_000028 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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASF1A NM_014034.2 ?/. - c.*23958T>A r.(=) p.(=)
MCM9 NM_153255.4 ?/. - c.152A>T r.(?) p.(Asn51Ile)


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