Variant #0000469318 (NC_000002.11:g.47705451G>C, NM_000251.2:c.2251G>C (MSH2))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47705451G>C |
DNA change (hg38) |
g.47478312G>C |
Published as |
- |
ISCN |
- |
DB-ID |
MSH2_001434 See all 3 reported entries |
Variant remarks |
Insight class: 4 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
InSiGHT - John-Paul Plazzer |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |
Date created |
2019-03-15 08:24:57 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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