Variant #0000089880 (NC_000006.11:g.6266847C>T, NM_000129.3:c.515G>A (F13A1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6266847C>T |
| DNA change (hg38) |
g.6266614C>T |
| Published as |
Arg171Gln |
| ISCN |
- |
| DB-ID |
F13A1_000010 |
| 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) |
3.0E-5 View details |
| Owner |
Arijit Biswas |
| Database submission license |
No license selected |
| Created by |
Arijit Biswas |
| Date created |
2016-02-24 13:52:29 +01:00 (CET) |
| Date last edited |
2019-07-09 13:56:51 +02:00 (CEST) |

Variant on transcripts
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