Variant #0000728001 (NC_000021.8:g.47648418G>C, NM_003906.3:c.*6764C>G (MCM3AP))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47648418G>C
DNA change (hg38) g.46228504G>C
Published as LSS(NM_002340.6):c.110C>G (p.T37S)
ISCN -
DB-ID LSS_000026
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-06-03 15:49:46 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LSS NM_002340.5 ?/. - c.110C>G r.(?) p.(Thr37Ser)
MCM3AP NM_003906.3 ?/. - c.*6764C>G r.(=) p.(=)


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