Variant #0000805481 (NC_000011.9:g.95568531A>G, NM_016156.5:c.1855T>C (MTMR2))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.95568531A>G |
DNA change (hg38) |
- |
Published as |
MTMR2(NM_001243571.2):c.1639T>C (p.S547P), MTMR2(NM_016156.5):c.1855T>C (p.S619P) |
ISCN |
- |
DB-ID |
CEP57_000019 See all 2 reported entries |
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) |
0.00285 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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