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 International |
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) |

Variant on transcripts
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