Variant #0001015907 (NC_000021.8:g.47655302C>G, NM_003906.3:c.5823G>C (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.47655302C>G
DNA change (hg38) -
Published as MCM3AP(NM_003906.5):c.5823G>C (p.A1941=)
ISCN -
DB-ID MCM3AP_000056
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) 0.00055 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.5823G>C r.(?) p.(=)
MCM3AP-AS1 NR_002776.3 -?/. - n.24-5446C>G r.(?) -


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