Variant #0000187932 (NC_000023.10:g.21861409G>C, NM_015884.3:c.197G>C (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.21861409G>C
DNA change (hg38) g.21843291G>C
Published as -
ISCN -
DB-ID MBTPS2_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs5951639
Origin Germline
Segregation -
Frequency 0.00
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 20:03:31 +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.197G>C r.(?) p.(Arg66Pro)


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