Variant #0000821072 (NC_000007.13:g.6026709G>A)
| Individual ID |
00390082 |
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (!) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6026709G>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PMS2_000470 See all 5 reported entries |
| Variant remarks |
ACMG: PVS1, PS4_MOD, PM3, PM2_SUP |
| Reference |
PMID: 21618646, 22608206, 25856668, 31857677, 32906206, 20205264, 22608206 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Andreas Laner |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Andreas Laner |
| Date created |
2021-11-10 08:27:44 +01:00 (CET) |
| Date last edited |
2021-11-10 09:13:58 +01:00 (CET) |

Variant on transcripts
Screenings
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