SUCLG2
succinate-CoA ligase GDP-forming subunit beta
Summary
This gene encodes a GTP-specific beta subunit of succinyl-CoA synthetase. Succinyl-CoA synthetase catalyzes the reversible reaction involving the formation of succinyl-CoA and succinate. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 5 and 12. [provided by RefSeq, Apr 2010]
Known Variants131 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2471372749 | 3:67,411,064 | A/G | — | uncertain significance |
| rs1238768986 | 3:67,411,099 | G/A | — | uncertain significance |
| rs533021862 | 3:67,411,100 | C/T | — | uncertain significance |
| rs902320 | 3:67,411,103 | T/C | — | benign |
| rs1450965184 | 3:67,411,113 | G/T | — | likely benign |
| rs192811331 | 3:67,411,131 | A/T | — | uncertain significance |
| rs2471373060 | 3:67,411,143 | T/C | — | likely benign |
| rs1197351448 | 3:67,411,162 | A/G | — | uncertain significance |
| rs902321 | 3:67,411,166 | G/A | — | benign |
| rs17806888 | 3:67,416,322 | T/G | — | — |
| rs2363709 | 3:67,417,105 | G/T | — | — |
| rs115560420 | 3:67,425,963 | G/T | intron variant | — |
| rs35494829 | 3:67,426,281 | T/C | intron variant | benign |
| rs185820586 | 3:67,426,290 | G/A | — | benign |
| rs775468197 | 3:67,426,293 | G/A | — | likely benign |
| rs202094027 | 3:67,446,212 | T/A | — | — |
| rs6785193 | 3:67,448,331 | G/A | — | — |
| rs1552628 | 3:67,450,626 | A/G | intron variant | — |
| rs140259546 | 3:67,451,135 | G/A | — | benign |
| rs180701292 | 3:67,451,163 | C/T | — | uncertain significance |
| rs771272322 | 3:67,451,176 | G/C | — | uncertain significance |
| rs12492080 | 3:67,451,196 | C/T | — | likely benign |
| rs7623258 | 3:67,451,197 | G/A | — | benign |
| rs201519398 | 3:67,451,217 | T/C | — | uncertain significance |
| rs2471450376 | 3:67,451,218 | T/G | — | uncertain significance |
| rs375028356 | 3:67,451,232 | C/A | — | uncertain significance |
| rs115935149 | 3:67,451,239 | C/T | — | uncertain significance |
| rs1052001825 | 3:67,451,240 | G/A | — | likely benign |
| rs746608461 | 3:67,451,242 | T/C | — | uncertain significance |
| rs746196486 | 3:67,451,256 | T/C | — | uncertain significance |
| rs1244643139 | 3:67,451,268 | G/C | — | uncertain significance |
| rs1490265 | 3:67,452,043 | C/G | — | — |
| rs4856781 | 3:67,454,224 | G/C | intron variant | — |
| rs4132748 | 3:67,455,803 | T/A | — | — |
| rs62256378 | 3:67,457,033 | G/A | intron variant | — |
| rs6792584 | 3:67,531,388 | G/A | intron variant | — |
| rs376098444 | 3:67,546,217 | G/A | — | uncertain significance |
| rs1313425208 | 3:67,546,239 | G/A | — | uncertain significance |
| rs1575734776 | 3:67,546,243 | T/C | — | likely benign |
| rs9843840 | 3:67,546,244 | T/C | — | benign |
| rs749647393 | 3:67,546,266 | C/A | — | conflicting classifications of pathogenicity |
| rs879055875 | 3:67,546,275 | C/T | — | uncertain significance |
| rs200728731 | 3:67,546,314 | C/T | — | uncertain significance |
| rs764123964 | 3:67,546,325 | A/G | — | uncertain significance |
| rs368002457 | 3:67,546,327 | G/A | — | likely benign |
| rs748534811 | 3:67,546,376 | A/G | — | likely benign |
| rs2471170394 | 3:67,546,379 | T/A | — | likely benign |
| rs766151119 | 3:67,548,543 | A/G | — | likely benign |
| rs765589082 | 3:67,548,563 | C/G | — | uncertain significance |
| rs953821574 | 3:67,548,579 | C/A | — | uncertain significance |
| rs374846104 | 3:67,548,590 | T/C | — | uncertain significance |
| rs375502051 | 3:67,548,640 | T/C | — | likely benign |
| rs200619917 | 3:67,548,645 | C/T | — | uncertain significance |
| rs368671579 | 3:67,548,672 | G/A | — | uncertain significance |
| rs187102568 | 3:67,548,682 | G/A | — | likely benign |
| rs141728876 | 3:67,548,687 | C/T | — | uncertain significance |
| rs1356418280 | 3:67,548,733 | A/G | — | likely benign |
| rs750496212 | 3:67,559,215 | T/C | — | likely benign |
| rs754024917 | 3:67,559,239 | T/C | — | uncertain significance |
| rs143813883 | 3:67,559,272 | T/A | — | uncertain significance |
| rs781236366 | 3:67,559,281 | T/A | — | uncertain significance |
| rs775954354 | 3:67,559,310 | C/T | — | likely benign |
| rs575033997 | 3:67,568,658 | A/G | — | benign |
| rs772354781 | 3:67,568,664 | T/C | — | likely benign |
| rs188443251 | 3:67,568,691 | C/T | — | uncertain significance |
| rs545537865 | 3:67,568,692 | G/A | — | likely benign |
| rs115053242 | 3:67,568,698 | T/C | — | benign |
| rs748940563 | 3:67,568,714 | C/T | — | uncertain significance |
| rs558481326 | 3:67,568,721 | C/T | — | uncertain significance |
| rs201652728 | 3:67,568,723 | T/G | — | uncertain significance |
| rs902797961 | 3:67,568,730 | C/G | — | uncertain significance |
| rs773673191 | 3:67,568,739 | C/T | — | uncertain significance |
| rs371562448 | 3:67,568,746 | A/T | — | likely benign |
| rs1706066484 | 3:67,570,889 | C/G | — | likely benign |
| rs771143012 | 3:67,570,890 | C/T | — | likely benign |
| rs149709855 | 3:67,570,892 | G/A | — | likely benign |
| rs762913452 | 3:67,570,922 | G/A | — | uncertain significance |
| rs1219455450 | 3:67,570,934 | G/A | — | uncertain significance |
| rs781757897 | 3:67,570,949 | T/G | — | uncertain significance |
| rs61756471 | 3:67,570,954 | G/A | — | likely benign |
| rs757799757 | 3:67,570,959 | C/G | — | uncertain significance |
| rs200035351 | 3:67,570,981 | G/A | — | likely benign |
| rs756592317 | 3:67,570,984 | G/T | — | likely benign |
| rs370620811 | 3:67,570,991 | C/A | — | uncertain significance |
| rs148943214 | 3:67,570,997 | C/T | — | uncertain significance |
| rs1033381754 | 3:67,571,021 | G/T | — | uncertain significance |
| rs965683095 | 3:67,571,030 | G/T | — | uncertain significance |
| rs377359813 | 3:67,571,070 | G/A | — | benign |
| rs2107128779 | 3:67,571,078 | G/T | — | likely benign |
| rs368985813 | 3:67,578,546 | T/C | — | likely benign |
| rs2471230973 | 3:67,578,549 | A/G | — | likely benign |
| rs1414617054 | 3:67,578,559 | G/T | — | uncertain significance |
| rs200929532 | 3:67,578,596 | G/A | — | uncertain significance |
| rs2471231200 | 3:67,578,615 | T/C | — | uncertain significance |
| rs13318110 | 3:67,578,624 | C/T | — | benign |
| rs184314579 | 3:67,578,627 | G/A | — | benign |
| rs772832797 | 3:67,578,651 | G/C | — | likely benign |
| rs62256401 | 3:67,578,664 | C/T | — | benign |
| rs75375870 | 3:67,579,501 | C/G | — | benign |
| rs1706332864 | 3:67,579,513 | T/G | — | uncertain significance |
Showing 100 of 131 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.