FLT4
fms related receptor tyrosine kinase 4
Summary
This gene encodes a tyrosine kinase receptor for vascular endothelial growth factors C and D. The protein is thought to be involved in lymphangiogenesis and maintenance of the lymphatic endothelium. Mutations in this gene cause hereditary lymphedema type IA. [provided by RefSeq, Jul 2008]
Known Variants346 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6877011 | 5:180,029,471 | C/G | 3 prime UTR variant | — |
| rs113034305 | 5:180,030,132 | C/T | — | benign |
| rs143739828 | 5:180,030,221 | C/T | — | likely benign |
| rs2270519 | 5:180,030,231 | C/T | — | likely benign |
| rs201381663 | 5:180,030,233 | G/A | — | uncertain significance |
| rs781063816 | 5:180,030,251 | C/T | — | uncertain significance |
| rs201796032 | 5:180,030,278 | C/T | — | likely benign |
| rs774068221 | 5:180,030,279 | G/A | — | likely benign |
| rs759044121 | 5:180,030,283 | T/C | — | uncertain significance |
| rs2127781697 | 5:180,030,285 | G/T | — | likely pathogenic |
| rs200963530 | 5:180,030,291 | C/T | — | likely benign |
| rs766308772 | 5:180,030,307 | G/A | — | uncertain significance |
| rs307821 | 5:180,030,313 | C/A | missense variant | benign |
| rs79620092 | 5:180,030,322 | C/T | — | likely benign |
| rs745546499 | 5:180,030,323 | G/A | — | uncertain significance |
| rs115824945 | 5:180,030,325 | C/T | — | benign |
| rs773779407 | 5:180,030,335 | C/T | — | uncertain significance |
| rs2127781827 | 5:180,030,364 | G/A | — | uncertain significance |
| rs146806202 | 5:180,030,376 | C/G | — | likely benign |
| rs1164783220 | 5:180,030,391 | C/T | — | uncertain significance |
| rs190589696 | 5:180,030,861 | A/C | — | — |
| rs2387212 | 5:180,035,347 | C/T | — | benign |
| rs307833 | 5:180,035,504 | C/T | — | benign |
| rs307832 | 5:180,035,792 | T/C | — | benign |
| rs564100331 | 5:180,035,837 | C/T | — | likely benign |
| rs138599624 | 5:180,035,975 | C/T | — | likely benign |
| rs141496824 | 5:180,035,976 | G/A | — | likely benign |
| rs34371546 | 5:180,035,994 | G/A | — | benign |
| rs2480811153 | 5:180,035,996 | T/G | — | uncertain significance |
| rs775663376 | 5:180,035,999 | C/G | — | uncertain significance |
| rs2127787560 | 5:180,036,034 | C/T | — | likely pathogenic |
| rs1407525547 | 5:180,036,036 | A/G | — | likely benign |
| rs2480811749 | 5:180,036,037 | C/G | — | uncertain significance |
| rs1309404142 | 5:180,036,038 | T/A | — | uncertain significance |
| rs1761973773 | 5:180,036,040 | T/A | — | likely pathogenic |
| rs1761976155 | 5:180,036,048 | G/C | — | uncertain significance |
| rs115500587 | 5:180,036,180 | C/G | — | benign |
| rs11750658 | 5:180,036,239 | A/G | — | benign |
| rs2242221 | 5:180,036,318 | G/A | — | benign |
| rs2242219 | 5:180,036,871 | C/G | — | benign |
| rs2480817663 | 5:180,036,928 | G/A | — | uncertain significance |
| rs746207295 | 5:180,036,934 | T/C | — | uncertain significance |
| rs142649193 | 5:180,036,959 | C/A | — | uncertain significance |
| rs770911540 | 5:180,036,996 | C/T | — | uncertain significance |
| rs766960409 | 5:180,037,000 | C/A | — | uncertain significance |
| rs1565819 | 5:180,037,317 | C/T | — | benign |
| rs140710164 | 5:180,038,336 | G/A | — | likely benign |
| rs201698561 | 5:180,038,364 | G/A | — | uncertain significance |
| rs1189576922 | 5:180,038,407 | T/C | — | uncertain significance |
| rs2127791606 | 5:180,038,429 | C/T | — | likely benign |
| rs1581616817 | 5:180,038,443 | G/A | — | pathogenic |
| rs2127791680 | 5:180,038,446 | A/G | — | uncertain significance |
| rs370304760 | 5:180,038,451 | C/T | — | uncertain significance |
| rs762445498 | 5:180,038,461 | T/C | — | uncertain significance |
| rs775810969 | 5:180,038,471 | C/G | — | uncertain significance |
| rs744283 | 5:180,038,545 | A/G | — | benign |
| rs55900466 | 5:180,038,696 | T/C | — | benign |
| rs77067564 | 5:180,038,711 | C/T | — | benign |
| rs100659 | 5:180,039,187 | A/G | — | benign |
| rs377256001 | 5:180,039,485 | C/T | — | likely benign |
| rs2127794030 | 5:180,039,511 | G/A | — | likely benign |
| rs1363156880 | 5:180,039,518 | G/T | — | likely benign |
| rs144713414 | 5:180,039,524 | G/C | — | likely benign |
| rs1403607630 | 5:180,039,539 | G/C | — | uncertain significance |
| rs753200941 | 5:180,039,574 | T/G | — | uncertain significance |
| rs75614493 | 5:180,039,583 | C/T | — | likely benign |
| rs1130379 | 5:180,039,606 | T/C | — | benign |
| rs774089319 | 5:180,039,607 | G/C | — | uncertain significance |
| rs1762335528 | 5:180,040,032 | G/A | — | likely pathogenic |
| rs1554109707 | 5:180,040,051 | C/T | — | pathogenic |
| rs376188634 | 5:180,040,062 | C/T | — | uncertain significance |
| rs121909652 | 5:180,040,101 | G/A | missense variant | pathogenic |
| rs2480842959 | 5:180,040,110 | C/T | — | pathogenic |
| rs80261784 | 5:180,040,740 | T/C | — | benign |
| rs2242217 | 5:180,040,918 | A/G | — | benign |
| rs421662 | 5:180,041,001 | G/C | — | benign |
| rs366388 | 5:180,041,008 | T/C | — | benign |
| rs121909656 | 5:180,041,083 | C/T | missense variant | pathogenic |
| rs2127797353 | 5:180,041,101 | A/G | — | uncertain significance |
| rs781402372 | 5:180,041,110 | C/T | — | uncertain significance |
| rs1376446971 | 5:180,041,137 | C/T | — | uncertain significance |
| rs150040385 | 5:180,041,138 | G/A | — | likely benign |
| rs121909655 | 5:180,041,142 | A/G | missense variant | pathogenic |
| rs1762428823 | 5:180,041,152 | G/A | — | uncertain significance |
| rs2480849793 | 5:180,041,157 | A/C | — | likely pathogenic |
| rs535681122 | 5:180,041,167 | G/C | — | uncertain significance |
| rs369575233 | 5:180,041,189 | C/T | — | uncertain significance |
| rs2934602 | 5:180,041,190 | A/G | — | likely benign |
| rs2934601 | 5:180,041,200 | T/G | — | likely benign |
| rs659268 | 5:180,041,208 | T/C | — | benign |
| rs2934600 | 5:180,041,242 | T/C | — | benign |
| rs2927582 | 5:180,041,274 | T/C | — | benign |
| rs56328898 | 5:180,041,316 | A/G | — | benign |
| rs2242216 | 5:180,041,491 | C/T | — | benign |
| rs55657009 | 5:180,043,330 | C/G | — | benign |
| rs771345898 | 5:180,043,377 | C/A | — | uncertain significance |
| rs774554521 | 5:180,043,378 | G/A | — | uncertain significance |
| rs1130378 | 5:180,043,388 | G/A | synonymous variant | benign |
| rs754111052 | 5:180,043,400 | G/A | — | likely benign |
| rs2480864921 | 5:180,043,405 | C/G | — | likely pathogenic |
Showing 100 of 346 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.