Variant #0000442808 (NC_000012.11:g.111353547G>T, NM_000432.3:c.141C>A (MYL2))
| Chromosome |
12 |
| Allele |
Parent #1 |
| 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.111353547G>T |
| DNA change (hg38) |
g.110915743G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MYL2_000004 See all 5 reported entries |
| Variant remarks |
expression cloning |
| Reference |
PubMed: Szczesna-Cordary |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00017 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2012-03-26 16:34:45 +02:00 (CEST) |
| Date last edited |
2020-07-03 09:51:14 +02:00 (CEST) |

Variant on transcripts
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