Variant #0000187937 (NC_000023.10:g.21863403C>T, NM_015884.3:c.339C>T (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.21863403C>T
DNA change (hg38) g.21845285C>T
Published as -
ISCN -
DB-ID MBTPS2_000009
Variant remarks Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID rs7063422
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBTPS2 NM_015884.3 ?/. 3 c.339C>T r.(?) p.(=)


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