Variant #0000187935 (NC_000023.10:g.21862918G>A, NC_000023.10(NM_015884.3):c.225-371G>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.21862918G>A
DNA change (hg38) g.21844800G>A
Published as -
ISCN -
DB-ID MBTPS2_000007
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs7057211
Origin Germline
Segregation -
Frequency 0.00-0.002
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 2017-08-08 20:04:31 +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.225-371G>A r.(?) p.(=)


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