Variant #0001025167 (NC_000006.11:g.119245202C>T, NM_153255.4:c.395G>A (MCM9))

Chromosome 6
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.119245202C>T
DNA change (hg38) -
Published as MCM9(NM_017696.3):c.395G>A (p.R132Q)
ISCN -
DB-ID ASF1A_000044
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) 6.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +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.*16423C>T r.(=) p.(=)
MCM9 NM_153255.4 -?/. - c.395G>A r.(?) p.(Arg132Gln)


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