Variant #0000291747 (NC_000015.9:g.90320146G>A, NM_001039958.1:c.558G>A (MESP2))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.90320146G>A |
DNA change (hg38) |
g.89776915G>A |
Published as |
MESP2(NM_001039958.2):c.558G>A (p.Q186=) |
ISCN |
- |
DB-ID |
MESP2_000004 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-07 09:38:45 +02:00 (CEST) |

Variant on transcripts
|