Variant #0000328768 (NC_000021.8:g.47703734G>A, NM_003906.3:c.1238C>T (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.47703734G>A
DNA change (hg38) g.46283820G>A
Published as MCM3AP(NM_003906.3):c.1238C>T (p.(Pro413Leu))
ISCN -
DB-ID MCM3AP_000012
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) 0.00835 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCM3AP NM_003906.3 -?/. - c.1238C>T r.(?) p.(Pro413Leu)
C21orf58 NM_058180.3 -?/. - c.*18179C>T r.(=) p.(=)
YBEY NM_058181.1 -?/. - c.-2962G>A r.(?) p.(=)


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