F2R
coagulation factor II thrombin receptor
Summary
Coagulation factor II receptor is a 7-transmembrane receptor involved in the regulation of thrombotic response. Proteolytic cleavage leads to the activation of the receptor. F2R is a G-protein coupled receptor family member. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2227744 | 5:76,010,349 | G/A | upstream gene variant | — |
| rs32934 | 5:76,010,706 | C/T | upstream gene variant | — |
| rs184688493 | 5:76,011,795 | C/G | — | — |
| rs2227745 | 5:76,012,064 | G/A | — | benign |
| rs1748341585 | 5:76,012,161 | C/T | — | uncertain significance |
| rs253061 | 5:76,014,000 | C/A | upstream gene variant | — |
| rs37243 | 5:76,014,319 | G/A | regulatory region variant | — |
| rs2227831 | 5:76,023,494 | A/G | intron variant | — |
| rs253072 | 5:76,024,819 | A/G | intron variant | — |
| rs75652818 | 5:76,026,356 | G/A | intron variant | — |
| rs153311 | 5:76,027,823 | A/T | — | — |
| rs168753 | 5:76,028,124 | A/G | — | — |
| rs149168216 | 5:76,028,164 | A/G | — | benign |
| rs2480069904 | 5:76,028,411 | A/G | — | uncertain significance |
| rs777014666 | 5:76,028,420 | A/G | — | uncertain significance |
| rs546007149 | 5:76,028,423 | G/C | — | uncertain significance |
| rs5894 | 5:76,028,566 | T/G | synonymous variant | benign |
| rs752467852 | 5:76,028,642 | A/G | — | uncertain significance |
| rs761939723 | 5:76,028,676 | A/G | — | uncertain significance |
| rs752508356 | 5:76,028,690 | C/A | — | uncertain significance |
| rs758373073 | 5:76,028,715 | C/T | — | uncertain significance |
| rs139693607 | 5:76,028,788 | G/A | — | benign |
| rs2480071208 | 5:76,028,822 | C/T | — | uncertain significance |
| rs1051926439 | 5:76,028,840 | G/A | — | uncertain significance |
| rs756717676 | 5:76,028,848 | C/T | — | likely benign |
| rs1055103 | 5:76,028,852 | G/T | — | uncertain significance |
| rs146829790 | 5:76,029,192 | A/G | — | benign |
| rs1748718333 | 5:76,029,201 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.