Variant #0000442664 (NC_000002.11:g.190926945C>T, NC_000002.11(NM_005259.2):c.373+5G>A (MSTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.190926945C>T
DNA change (hg38) g.190062219C>T
Published as IVS1+5G>A
ISCN -
DB-ID MSTN_000013 See all 7 reported entries
Variant remarks gene cloned and expressed in CHO cells, MSTN virtually absent from medium
Reference PubMed: Schuelke 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site AccI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2008-12-14 17:00:08 +01:00 (CET)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSTN NM_005259.2 +/. 1i c.373+5G>A r.[373_374ins373+1_373+108; 373+5g>a] p.Ser125Cysfs*3


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