Variant #0000426135 (NC_000002.11:g.47637246A>G, NM_000251.2:c.380A>G (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47637246A>G |
| DNA change (hg38) |
g.47410107A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH2_000031 See all 49 reported entries |
| Variant remarks |
partial skipping of exon 3 |
| Reference |
PubMed: Tricarico 2017 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00548 View details |
| Owner |
Alexandra Martins |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
InSiGHT - John-Paul Plazzer |
| Date created |
2016-09-14 07:49:46 +02:00 (CEST) |
| Date last edited |
2020-07-14 22:00:36 +02:00 (CEST) |

Variant on transcripts
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