Variant #0001005852 (NC_000021.8:g.47704855T>C, NM_003906.3:c.346A>G (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.47704855T>C
DNA change (hg38) -
Published as MCM3AP(NM_003906.3):c.346A>G (p.(Thr116Ala))
ISCN -
DB-ID C21orf58_000018
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.346A>G r.(?) p.(Thr116Ala)
C21orf58 NM_058180.3 -?/. - c.*17058A>G r.(=) p.(=)
YBEY NM_058181.1 -?/. - c.-1841T>C r.(?) p.(=)


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