Variant #0000415495 (NC_000007.13:g.6048650T>C, NM_000535.6:c.1A>G (PMS2))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6048650T>C |
| DNA change (hg38) |
g.6009019T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PMS2_000256 See all 17 reported entries |
| Variant remarks |
ICCON data, Westmead, NSW |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
InSiGHT - John-Paul Plazzer |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
InSiGHT - John-Paul Plazzer |
| Date created |
2016-07-07 12:00:00 +02:00 (CEST) |
| Date last edited |
2020-06-22 14:33:53 +02:00 (CEST) |

Variant on transcripts
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