Variant #0000187934 (NC_000023.10:g.21861487G>A, NC_000023.10(NM_015884.3):c.224+51G>A (MBTPS2))

Chromosome X
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.21861487G>A
DNA change (hg38) g.21843369G>A
Published as -
ISCN -
DB-ID MBTPS2_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs3213452
Origin Germline
Segregation -
Frequency 0.00-0.005
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 2017-08-08 20:03:31 +02:00 (CEST)
Date last edited 2020-07-17 20:12:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBTPS2 NM_015884.3 ?/. 2i c.224+51G>A r.(?) p.(=)


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