Variant #0000802286 (NC_000006.11:g.119137147T>C, NM_153255.4:c.*95642A>G (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.119137147T>C
DNA change (hg38) -
Published as MCM9(NM_017696.2):c.2272A>G (p.(Thr758Ala)), MCM9(NM_017696.3):c.2272A>G (p.T758A)
ISCN -
DB-ID ASF1A_000013 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) 0.02794 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 2021-09-17 14:40:49 +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.-78431T>C r.(?) p.(=)
MCM9 NM_153255.4 -/. - c.*95642A>G r.(=) p.(=)


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