SUGCT
succinyl-CoA:glutarate-CoA transferase
Summary
This gene encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Mutations in this gene are associated with glutaric aciduria type III. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]
Known Variants138 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs137853117 | 7:40,172,768 | T/C | missense variant | pathogenic |
| rs869312900 | 7:40,173,827 | C/T | — | pathogenic |
| rs587776532 | 7:40,173,890 | — | — | pathogenic |
| rs202171580 | 7:40,174,614 | C/T | — | uncertain significance |
| rs1787597178 | 7:40,174,626 | G/C | — | uncertain significance |
| rs907452137 | 7:40,174,644 | G/A | — | uncertain significance |
| rs7793074 | 7:40,174,673 | C/A | — | benign |
| rs1266989400 | 7:40,174,676 | C/T | — | likely benign |
| rs868059002 | 7:40,174,678 | G/A | — | uncertain significance |
| rs1418509936 | 7:40,174,686 | G/T | — | uncertain significance |
| rs370031397 | 7:40,174,711 | C/T | — | conflicting classifications of pathogenicity |
| rs1881684 | 7:40,196,444 | G/A | downstream gene variant | — |
| rs7778061 | 7:40,220,412 | T/C | — | benign |
| rs116844030 | 7:40,220,475 | A/G | — | benign |
| rs2036041 | 7:40,220,507 | C/G | — | benign |
| rs372464576 | 7:40,220,548 | A/G | — | uncertain significance |
| rs193023834 | 7:40,220,571 | A/C | — | conflicting classifications of pathogenicity |
| rs751997717 | 7:40,220,605 | T/C | — | likely benign |
| rs58068135 | 7:40,220,725 | G/A | — | benign |
| rs2484565697 | 7:40,221,573 | G/A | — | uncertain significance |
| rs199580919 | 7:40,221,593 | T/A | — | uncertain significance |
| rs2484566419 | 7:40,221,601 | C/A | — | uncertain significance |
| rs754987090 | 7:40,221,624 | C/G | — | uncertain significance |
| rs138579332 | 7:40,227,912 | G/A | — | benign |
| rs644966 | 7:40,228,028 | A/T | — | benign |
| rs774925854 | 7:40,228,055 | C/A | — | benign |
| rs78060149 | 7:40,228,078 | A/T | — | benign |
| rs200690632 | 7:40,228,112 | G/C | — | uncertain significance |
| rs747590282 | 7:40,228,114 | A/G | — | uncertain significance |
| rs1308632780 | 7:40,228,121 | G/A | — | uncertain significance |
| rs913673123 | 7:40,228,132 | G/T | — | uncertain significance |
| rs2484630604 | 7:40,228,154 | A/T | — | likely benign |
| rs945008885 | 7:40,228,156 | C/T | — | uncertain significance |
| rs137852862 | 7:40,228,168 | C/T | stop gained | pathogenic |
| rs115327068 | 7:40,228,235 | A/T | — | benign |
| rs7776964 | 7:40,228,890 | A/G | — | benign |
| rs7776967 | 7:40,228,898 | A/G | — | benign |
| rs4720354 | 7:40,229,072 | G/A | — | benign |
| rs571652463 | 7:40,229,125 | A/T | — | likely benign |
| rs10236765 | 7:40,229,127 | A/T | — | benign |
| rs57321637 | 7:40,229,129 | T/A | — | likely benign |
| rs1322360615 | 7:40,229,141 | A/G | — | uncertain significance |
| rs2150734056 | 7:40,229,142 | G/C | — | likely pathogenic |
| rs1785768182 | 7:40,229,144 | G/A | — | uncertain significance |
| rs2484642920 | 7:40,229,170 | A/G | — | uncertain significance |
| rs77071634 | 7:40,234,415 | G/T | — | benign |
| rs753443747 | 7:40,234,631 | T/C | — | likely benign |
| rs138102615 | 7:40,234,653 | A/C | — | conflicting classifications of pathogenicity |
| rs7807456 | 7:40,234,923 | C/T | — | benign |
| rs76667176 | 7:40,277,228 | T/C | — | benign |
| rs137852861 | 7:40,277,263 | C/T | stop gained | pathogenic |
| rs375255318 | 7:40,277,267 | C/T | — | uncertain significance |
| rs201433905 | 7:40,277,288 | C/T | — | uncertain significance |
| rs1182710002 | 7:40,277,302 | C/T | — | likely benign |
| rs186721582 | 7:40,289,816 | G/A | intron variant | — |
| rs7778070 | 7:40,289,864 | A/T | — | — |
| rs75868549 | 7:40,314,055 | A/C | — | benign |
| rs778128318 | 7:40,314,120 | T/C | — | likely benign |
| rs1792330820 | 7:40,314,128 | G/A | — | uncertain significance |
| rs1792331371 | 7:40,314,132 | A/C | — | likely benign |
| rs769764892 | 7:40,314,155 | C/T | — | uncertain significance |
| rs12669315 | 7:40,314,165 | G/A | — | benign |
| rs573495001 | 7:40,314,180 | T/G | — | likely benign |
| rs1792336570 | 7:40,314,181 | A/T | — | uncertain significance |
| rs2485335166 | 7:40,314,217 | A/G | — | uncertain significance |
| rs4637704 | 7:40,314,243 | G/A | — | benign |
| rs114366175 | 7:40,314,353 | A/G | — | benign |
| rs17171670 | 7:40,333,942 | T/G | intron variant | — |
| rs79849677 | 7:40,356,154 | T/C | — | benign |
| rs73135029 | 7:40,356,305 | A/G | — | benign |
| rs10245165 | 7:40,356,315 | A/T | — | benign |
| rs1421397043 | 7:40,356,351 | C/A | — | likely benign |
| rs779940170 | 7:40,356,371 | T/C | — | uncertain significance |
| rs754828574 | 7:40,356,385 | A/G | — | likely benign |
| rs375435686 | 7:40,356,416 | C/T | — | uncertain significance |
| rs192547523 | 7:40,356,417 | G/A | — | uncertain significance |
| rs185036245 | 7:40,356,418 | T/C | — | benign |
| rs28477494 | 7:40,356,717 | G/A | — | benign |
| rs28637571 | 7:40,356,724 | G/A | — | benign |
| rs186166891 | 7:40,406,876 | A/T | intron variant | — |
| rs10234636 | 7:40,427,617 | T/G | — | — |
| rs9648487 | 7:40,430,299 | G/C | intron variant | — |
| rs77024938 | 7:40,430,792 | G/C | intron variant | — |
| rs76206723 | 7:40,447,971 | G/C | — | — |
| rs12538229 | 7:40,460,129 | C/A | — | — |
| rs4379368 | 7:40,466,200 | C/T | intron variant | — |
| rs1319467 | 7:40,477,363 | A/C | — | — |
| rs12666860 | 7:40,488,852 | A/C | — | benign |
| rs368009272 | 7:40,488,908 | A/G | — | uncertain significance |
| rs930000846 | 7:40,488,944 | C/G | — | uncertain significance |
| rs538044899 | 7:40,488,965 | A/G | — | likely benign |
| rs7809620 | 7:40,489,083 | T/C | — | benign |
| rs773683721 | 7:40,498,683 | T/A | — | likely benign |
| rs6960628 | 7:40,498,693 | C/A | — | benign |
| rs775757170 | 7:40,498,706 | G/T | — | uncertain significance |
| rs763107282 | 7:40,498,730 | T/C | — | uncertain significance |
| rs137852860 | 7:40,498,796 | C/T | missense variant | pathogenic |
| rs3779135 | 7:40,498,829 | G/T | — | benign |
| rs192180976 | 7:40,535,879 | T/C | — | likely benign |
| rs570248035 | 7:40,644,379 | G/C | — | — |
Showing 100 of 138 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.