Variant #0000187923 (NC_000023.10:g.21886591G>T, NM_015884.3:c.677G>T (MBTPS2))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.21886591G>T
DNA change (hg38) g.21868473G>T
Published as -
ISCN -
DB-ID MBTPS2_000020 See all 4 reported entries
Variant remarks cloned in EYFP fusion construc in pcDNA3.1; CHO expression limited complementation SP2 deficiency
Reference PubMed: Oeffner 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Emmelien Aten
Database submission license No license selected
Created by Emmelien Aten
Date created 2009-08-18 09:19:58 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBTPS2 NM_015884.3 +?/. 6 c.677G>T r.(?) p.Trp226Leu


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