Variant #0000187933 (NC_000023.10:g.21861434A>G, NM_015884.3:c.222A>G (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.21861434A>G
DNA change (hg38) g.21843316A>G
Published as -
ISCN -
DB-ID MBTPS2_000005 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs3213451
Origin Germline
Segregation -
Frequency 0.24-0.57
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.42828 View details
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 20:03:31 +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 ?/. 2 c.222A>G r.(?) p.(=)


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