Variant #0001035433 (NC_000006.11:g.119136853C>T, NM_153255.4:c.*95936G>A (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.119136853C>T
DNA change (hg38) -
Published as MCM9(NM_017696.2):c.2566G>A (p.A856T), MCM9(NM_017696.3):c.2566G>A (p.A856T)
ISCN -
DB-ID ASF1A_000001 See all 3 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) 0.00053 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 2025-05-05 21:14:00 +02:00 (CEST)
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.-78725C>T r.(?) p.(=)
MCM9 NM_153255.4 ?/. - c.*95936G>A r.(=) p.(=)


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