Variant #0000298948 (NC_000007.13:g.6026607T>A, NM_000535.6:c.1789A>T (PMS2))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6026607T>A |
| DNA change (hg38) |
g.5986976T>A |
| Published as |
PMS2(NM_000535.5):c.1789A>T (p.(Thr597Ser), p.Thr597Ser, p.T597S), PMS2(NM_000535.7):c.1789A>T (p.T597S) |
| ISCN |
- |
| DB-ID |
PMS2_000145 See all 24 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00842 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|