Variant #0000984058 (NC_000021.8:g.47674741_47674742insC, NM_003906.3:c.3949_3950insG (MCM3AP))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47674741_47674742insC
DNA change (hg38) -
Published as MCM3AP(NM_003906.5):c.3949_3950insG (p.N1317Rfs*19)
ISCN -
DB-ID MCM3AP_000052
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-04-19 20:27:30 +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     
MCM3AP NM_003906.3 +?/. - c.3949_3950insG r.(?) p.(Asn1317Argfs*19)


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