Variant #0000736813 (NC_000017.10:g.7352014C>T)
| Individual ID |
00335954 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS (!) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.7352014C>T |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CHRNB1_000004 See all 4 reported entries |
| Variant remarks |
ACMG: PM2_Sup, PM3, PP3: class 3; / NM_000747.3:c.727C>T chr17:7352014 p.(Arg243Cys) |
| Reference |
PMID: 29395675; PMID: 17686188 |
| ClinVar ID |
ClinVar-000448999 |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Andreas Laner |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Andreas Laner |
| Date created |
2021-03-10 14:49:45 +01:00 (CET) |
| Date last edited |
2021-03-17 14:59:14 +01:00 (CET) |

Variant on transcripts
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