Variant #0000426413 (NC_000002.11:g.47672729T>C, NM_000251.2:c.1319T>C (MSH2))
Chromosome |
2 |
Allele |
Unknown |
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.47672729T>C |
DNA change (hg38) |
g.47445590T>C |
Published as |
L440P |
ISCN |
- |
DB-ID |
MSH2_000720 See all 14 reported entries |
Variant remarks |
{GR:167} |
Reference |
PubMed: Gammie 2007 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Rolf Sijmons |
Database submission license |
No license selected |
Created by |
Rolf Sijmons |
Date created |
2009-02-06 12:00:00 +01:00 (CET) |
Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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