Variant #0000294046 (NC_000007.13:g.6045634T>C, NM_000535.6:c.52A>G (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.6045634T>C |
| DNA change (hg38) |
g.6006003T>C |
| Published as |
PMS2(NM_000535.5):c.52A>G (p.(Ile18Val), p.Ile18Val, p.I18V), PMS2(NM_000535.7):c.52A>G (p.I18V) |
| ISCN |
- |
| DB-ID |
PMS2_000009 See all 23 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) |
0.00906 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| 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
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