Variant #0000328765 (NC_000021.8:g.47671440C>A, NC_000021.8(NM_003906.3):c.4290+3G>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.47671440C>A
DNA change (hg38) g.46251526C>A
Published as MCM3AP(NM_003906.3):c.4290+3G>T (p.?)
ISCN -
DB-ID MCM3AP_000007
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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 ?/. - c.4290+3G>T r.spl? p.?
MCM3AP-AS1 NR_002776.3 ?/. - n.2150C>A r.(?) -


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