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 3 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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