Variant #0000089879 (NC_000006.11:g.6266859T>C, NM_000129.3:c.503A>G (F13A1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6266859T>C |
| DNA change (hg38) |
g.6266626T>C |
| Published as |
Tyr167Cys |
| ISCN |
- |
| DB-ID |
F13A1_000011 |
| Variant remarks |
expression cloning COS-1 cells |
| Reference |
PubMed: Thomas 2016, Journal: Thomas 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Arijit Biswas |
| Database submission license |
No license selected |
| Created by |
Arijit Biswas |
| Date created |
2016-02-24 13:43:37 +01:00 (CET) |
| Date last edited |
2019-07-09 13:56:51 +02:00 (CEST) |

Variant on transcripts
|