FOXP1
forkhead box P1
Summary
This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Known Variants695 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs185295985 | 3:71,004,985 | A/G | — | benign |
| rs532852561 | 3:71,006,061 | C/G | — | uncertain significance |
| rs577920948 | 3:71,007,355 | A/T | — | uncertain significance |
| rs886058853 | 3:71,007,782 | G/A | — | uncertain significance |
| rs373960974 | 3:71,008,392 | C/G | — | uncertain significance |
| rs2032597380 | 3:71,008,399 | C/T | — | likely benign |
| rs931493078 | 3:71,008,401 | C/T | — | likely benign |
| rs2032601929 | 3:71,008,408 | T/C | — | likely benign |
| rs2106854508 | 3:71,008,410 | C/T | — | likely benign |
| rs368167189 | 3:71,008,412 | C/T | — | conflicting classifications of pathogenicity |
| rs774470005 | 3:71,008,418 | C/T | — | uncertain significance |
| rs772162873 | 3:71,008,431 | G/A | — | likely benign |
| rs2032611709 | 3:71,008,443 | A/G | — | likely benign |
| rs759325225 | 3:71,008,450 | A/G | — | uncertain significance |
| rs927383097 | 3:71,008,455 | T/C | — | likely benign |
| rs2544830886 | 3:71,008,457 | G/C | — | uncertain significance |
| rs2106856835 | 3:71,008,464 | G/A | — | likely benign |
| rs2544831054 | 3:71,008,467 | G/A | — | likely benign |
| rs762475508 | 3:71,008,468 | G/A | — | conflicting classifications of pathogenicity |
| rs2106856969 | 3:71,008,469 | C/T | — | uncertain significance |
| rs1341867805 | 3:71,008,471 | G/A | — | uncertain significance |
| rs2544831333 | 3:71,008,475 | T/C | — | uncertain significance |
| rs183825221 | 3:71,008,477 | A/C | — | benign |
| rs2032627155 | 3:71,008,480 | A/G | — | uncertain significance |
| rs2106857321 | 3:71,008,483 | G/T | — | uncertain significance |
| rs895839462 | 3:71,008,484 | A/T | — | uncertain significance |
| rs2106857450 | 3:71,008,486 | A/G | — | uncertain significance |
| rs756987886 | 3:71,008,496 | C/T | — | uncertain significance |
| rs2544831873 | 3:71,008,498 | G/C | — | uncertain significance |
| rs2544831944 | 3:71,008,504 | T/A | — | uncertain significance |
| rs541340602 | 3:71,008,511 | C/T | — | uncertain significance |
| rs991506093 | 3:71,008,529 | C/T | — | uncertain significance |
| rs749771909 | 3:71,008,530 | G/A | — | conflicting classifications of pathogenicity |
| rs113891864 | 3:71,008,536 | A/T | — | likely benign |
| rs2106858982 | 3:71,008,541 | G/A | — | uncertain significance |
| rs748164903 | 3:71,008,546 | G/A | — | likely benign |
| rs187666567 | 3:71,008,547 | A/G | — | likely benign |
| rs2544833002 | 3:71,008,552 | A/T | — | likely benign |
| rs7639736 | 3:71,008,557 | A/C | — | benign |
| rs1288487138 | 3:71,008,558 | A/G | — | likely benign |
| rs192056954 | 3:71,008,559 | G/A | — | benign |
| rs139747537 | 3:71,008,679 | C/T | — | likely benign |
| rs11928045 | 3:71,014,836 | T/C | — | benign |
| rs17008086 | 3:71,014,892 | T/C | — | benign |
| rs7638391 | 3:71,015,021 | G/T | — | benign |
| rs774095805 | 3:71,015,030 | A/G | — | likely benign |
| rs761406403 | 3:71,015,033 | A/G | — | likely benign |
| rs771667463 | 3:71,015,034 | T/A | — | uncertain significance |
| rs1553656383 | 3:71,015,036 | C/A | — | likely pathogenic |
| rs1553656387 | 3:71,015,040 | C/A | — | pathogenic |
| rs772816590 | 3:71,015,042 | C/A | — | conflicting classifications of pathogenicity |
| rs766116383 | 3:71,015,043 | G/A | — | likely benign |
| rs2544928140 | 3:71,015,047 | T/C | — | uncertain significance |
| rs754932182 | 3:71,015,051 | T/C | — | uncertain significance |
| rs2544928204 | 3:71,015,058 | T/A | — | uncertain significance |
| rs2107012031 | 3:71,015,071 | C/T | — | uncertain significance |
| rs1391157769 | 3:71,015,072 | T/C | — | likely benign |
| rs2544928476 | 3:71,015,076 | A/C | — | uncertain significance |
| rs1313753034 | 3:71,015,079 | C/G | — | uncertain significance |
| rs1323763108 | 3:71,015,081 | C/T | — | uncertain significance |
| rs1231630526 | 3:71,015,082 | G/A | — | likely benign |
| rs1272638140 | 3:71,015,087 | T/C | — | uncertain significance |
| rs2034670485 | 3:71,015,089 | T/C | — | uncertain significance |
| rs758540752 | 3:71,015,095 | T/A | — | uncertain significance |
| rs777876809 | 3:71,015,097 | C/A | — | conflicting classifications of pathogenicity |
| rs2544928948 | 3:71,015,099 | C/T | — | likely benign |
| rs757539300 | 3:71,015,104 | G/A | — | likely benign |
| rs147537388 | 3:71,015,105 | C/T | — | likely benign |
| rs749121207 | 3:71,015,108 | C/G | — | uncertain significance |
| rs768285337 | 3:71,015,109 | G/A | — | likely benign |
| rs778939994 | 3:71,015,114 | G/A | — | likely benign |
| rs748075031 | 3:71,015,122 | C/T | — | likely benign |
| rs2034676627 | 3:71,015,123 | G/A | — | uncertain significance |
| rs2034678143 | 3:71,015,127 | T/A | — | likely benign |
| rs2544929661 | 3:71,015,128 | G/A | — | uncertain significance |
| rs373809702 | 3:71,015,129 | C/T | — | likely benign |
| rs760260048 | 3:71,015,130 | G/A | — | likely benign |
| rs970358469 | 3:71,015,132 | T/C | — | uncertain significance |
| rs2544929872 | 3:71,015,137 | A/G | — | uncertain significance |
| rs2544929895 | 3:71,015,140 | T/C | — | benign |
| rs2544929972 | 3:71,015,144 | C/T | — | uncertain significance |
| rs1413171367 | 3:71,015,145 | C/G | — | likely benign |
| rs1292897246 | 3:71,015,147 | G/C | — | uncertain significance |
| rs2034683194 | 3:71,015,152 | G/T | — | uncertain significance |
| rs1364685833 | 3:71,015,158 | C/G | — | uncertain significance |
| rs201446635 | 3:71,015,162 | T/C | — | likely benign |
| rs2544930420 | 3:71,015,164 | G/C | — | uncertain significance |
| rs765482675 | 3:71,015,166 | A/G | — | likely benign |
| rs202173892 | 3:71,015,168 | C/T | — | likely benign |
| rs764576604 | 3:71,015,169 | G/A | — | likely benign |
| rs757267242 | 3:71,015,180 | G/T | — | uncertain significance |
| rs1423437984 | 3:71,015,183 | G/A | — | uncertain significance |
| rs750569571 | 3:71,015,190 | A/G | — | likely benign |
| rs1038860326 | 3:71,015,191 | T/C | — | uncertain significance |
| rs756328632 | 3:71,015,193 | C/G | — | likely benign |
| rs2034694477 | 3:71,015,194 | T/C | — | uncertain significance |
| rs2034696345 | 3:71,015,198 | C/T | — | uncertain significance |
| rs2544931449 | 3:71,015,199 | C/T | — | uncertain significance |
| rs371033424 | 3:71,015,221 | A/C | — | likely benign |
| rs111425991 | 3:71,019,708 | G/A | — | likely benign |
Showing 100 of 695 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.