Variant #0000075725 (NC_000021.8:g.47703645G>A, NM_003906.3:c.1327C>T (MCM3AP))

Chromosome 21
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.47703645G>A
DNA change (hg38) g.46283731G>A
Published as -
ISCN -
DB-ID MCM3AP_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs202234966
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Timo Heß
Database submission license No license selected
Created by Timo Heß
Date created 2015-08-03 13:18:30 +02:00 (CEST)
Date last edited 2015-09-06 21:54:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCM3AP NM_003906.3 ?/. 2 c.1327C>T r.(?) p.(Pro443Ser)



Screenings

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