Variant #0000866697 (NC_000021.8:g.47704253G>C, NM_003906.3:c.948C>G (MCM3AP))

Chromosome 21
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47704253G>C
DNA change (hg38) -
Published as MCM3AP(NM_003906.5):c.948C>G (p.S316=)
ISCN -
DB-ID C21orf58_000011
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) 0.00429 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 2022-05-09 16:01:56 +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.948C>G r.(?) p.(Ser316=)
C21orf58 NM_058180.3 -/. - c.*17660C>G r.(=) p.(=)
YBEY NM_058181.1 -/. - c.-2443G>C r.(?) p.(=)


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