Variant #0000074688 (NC_000007.13:g.6029429A>T, NC_000007.13(NM_000535.6):c.1144+2T>A (PMS2))
| Chromosome |
7 |
| 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.6029429A>T |
| DNA change (hg38) |
g.5989798A>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PMS2_000040 See all 5 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 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2015-07-20 15:58:19 +02:00 (CEST) |
| Date last edited |
2019-02-22 12:22:30 +01:00 (CET) |

Variant on transcripts
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