Variant #0000693085 (NC_000021.8:g.47664746C>T, NM_003906.3:c.5013G>A (MCM3AP))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47664746C>T
DNA change (hg38) -
Published as MCM3AP(NM_003906.4):c.5013G>A (p.P1671=), MCM3AP(NM_003906.5):c.5013G>A (p.P1671=)
ISCN -
DB-ID MCM3AP_000029 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) 0.0025 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
MCM3AP NM_003906.3 -?/. - c.5013G>A r.(?) p.(Pro1671=)
MCM3AP-AS1 NR_002776.3 -?/. - n.209+3813C>T r.(?) -


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