Variant #0000860135 (NC_000006.11:g.119234579T>C, NM_153255.4:c.911A>G (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.119234579T>C
DNA change (hg38) -
Published as MCM9(NM_017696.3):c.911A>G (p.N304S)
ISCN -
DB-ID MCM9_000001 See all 5 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) 0.00354 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 2022-05-09 15:51:19 +02:00 (CEST)
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.*5800T>C r.(=) p.(=)
MCM9 NM_153255.4 -?/. - c.911A>G r.(?) p.(Asn304Ser)


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