Variant #0000371357 (NC_000002.11:g.47630331A>G, MSH2(NM_000251.2):c.1A>G)
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47630331A>G |
DNA change (hg38) |
g.47403192A>G |
Published as |
- |
ISCN |
- |
DB-ID |
MSH2_001066 See all 7 reported entries |
Variant remarks |
Insight class: 3 |
Reference |
InSiGHT |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
InSiGHT - John-Paul Plazzer |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |

Variant on transcripts
|
|