Variant #0000951525 (NC_000021.8:g.47660867G>A, NM_003906.3:c.5491C>T (MCM3AP))

Chromosome 21
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.47660867G>A
DNA change (hg38) -
Published as MCM3AP(NM_003906.5):c.5491C>T (p.R1831C)
ISCN -
DB-ID MCM3AP_000048
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) 0.00253 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCM3AP NM_003906.3 -/. - c.5491C>T r.(?) p.(Arg1831Cys)
MCM3AP-AS1 NR_002776.3 -/. - n.143G>A r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.