Strain | Affected gene(s) | Types of mutations | Affected nucleotide(s) [Affected amino acid] |
---|---|---|---|
1827702 | cps2E | Missense | A61G [Thr21Ala] |
cps2I | Insertion | IS element: 33Â bp | |
cps2N | Deletion | 27Â bp | |
1090772 | cps2E | Missense | A61G [Thr21Ala] |
cps2F | Missense | A149G [Asp50Gly] | |
 | Missense | A1047T [Leu349Phe] | |
cps2I | Insertion | IS element: 33Â bp | |
cps2N | Deletion | 27Â bp | |
cps2O | Missense | C859A [Arg287Ser] | |
1160406 | cps27E | Missense | A506G [Asp169Gly] |
 | Missense | T508A [Ser170Thr] | |
 | Missense | A513T [Glu171Asp] | |
 | Missense | A522T [Lys174Asn] | |
 | Missense | A524T A525T [Lys175Ile] | |
 | Missense | A541C C543G [Ile181Leu] | |
 | Missense | A553G [Ile185Val] | |
 | Missense | G617T T618G [Ser206Met] | |
 |  | Missense | A623T [Tyr208Phe] |
 | Missense | T633G [Leu211Val] | |
 | Missense | C640T A642C [Leu214Phe] | |
 | Missense | A651T [Glu217Asp] | |
 | Missense | C692T [Ser231Leu] | |
 | Missense | G706A A708G [Ala236Thr] | |
 | Missense | G874A A876T [Val292Ile] | |
 | Missense | T905C [Val302Ala] | |
 | Missense | A922C A924G [Lys308Gln] | |
 | Missense | A941C G942A [Lys314Thr] | |
 | Missense | A967G [Ile323Val] | |
 | Missense | A997C G999C [Met333Leu] | |
 | Missense | G1000A C1001G T1002C [Ala334Ser] | |
 | Missense | A1174C A1175G [Lys392Arg] | |
 | Missense | G1186A G1187T T1188G [Gly396Met] | |
 | Missense | A1272C [Glu424Asp] | |
 | Missense | A1279C A1280G [Lys427Arg] | |
 | Missense | G1288T T1290A [Val430Leu] | |
 | Missense | A1292C [Glu431Ala] | |
 | Missense | G1324A A1326T [Val442Ile] | |
 | Missense | A1357T T1359G [Ile453Leu] | |
 | Missense | A1360T A1361T [Lys454Leu] | |
cps27F | Deletion | 27Â bp | |
 | Missense | A662T [His221Leu] | |
cps27G | Insertion | IS element: 21Â bp | |
cps27I | Missense | G483C [Trp161Cys] | |
 | Missense | C513A [Asp171Glu] | |
 | Missense | A611G [Gln204Arg] | |
cps27L | Deletion | 57Â bp | |
cps27M | Missense | C1373T C1374T [Ala458Val] | |
 | Missense | C1375T [Leu459Phe] |