Table 4

Newly acquired mutations in nitrogen regulatory protein C family (NRC) genes in the EN populations.

GenePopulationsMutation typeAllele frequency (%)Mutation positionNucleotide changeAmino-acid change
DVU2394EN3Deletion162497229−1: G2 amino acids changed
SNP592497736C → TGlu → Lys
EN5SNP162496979T → CTyr → Cys
EN6Deletion492497411−1: GFrameshift mutation
EN7Deletion1002497258−18: GCAATTCACGCACGTTGC6 amino acids loss
EN9Deletion362497708−19:GAACAGTTCGCTACGGGCCFrameshift mutation
Insertion112497728+12: GACCGCGGACAT4 amino acids inserted
DVU2395EN4Deletion1002499096−8: CGGCGAGCFrameshift mutation
EN8Insertion462498544+2: CG4 amino acids changed
262499078+14:CCTCATGCGCCACCFrameshift mutation
EN9Deletion542499384−1: TFrameshift mutation
EN10SNP152498363T → CSilent mutation
SNP232498737T → CLys → Glu
SNP452498935G → AGln → STOP
EN12SNP1002499244G → AGln → STOP
DVU2396EN1SNP202499926G → APro → Ser
SNP722500012G → TSer → STOP
EN2Deletion982499984−1: CFrameshift mutation
EN6Deletion422499735−1: CFrameshift mutation
DVU2402EN2SNP962507986G → AArg → Cys
DVU2405EN5SNP812510695C → AGlu → STOP
EN11Deletion1002510695−1: CFrameshift mutation
SNP1002510695C → TGlu → Lys
GenePopulationsMutation typeAllele frequency (%)Mutation positionNucleotide changeAmino-acid change
DVU2394EN3Deletion162497229−1: G2 amino acids changed
SNP592497736C → TGlu → Lys
EN5SNP162496979T → CTyr → Cys
EN6Deletion492497411−1: GFrameshift mutation
EN7Deletion1002497258−18: GCAATTCACGCACGTTGC6 amino acids loss
EN9Deletion362497708−19:GAACAGTTCGCTACGGGCCFrameshift mutation
Insertion112497728+12: GACCGCGGACAT4 amino acids inserted
DVU2395EN4Deletion1002499096−8: CGGCGAGCFrameshift mutation
EN8Insertion462498544+2: CG4 amino acids changed
262499078+14:CCTCATGCGCCACCFrameshift mutation
EN9Deletion542499384−1: TFrameshift mutation
EN10SNP152498363T → CSilent mutation
SNP232498737T → CLys → Glu
SNP452498935G → AGln → STOP
EN12SNP1002499244G → AGln → STOP
DVU2396EN1SNP202499926G → APro → Ser
SNP722500012G → TSer → STOP
EN2Deletion982499984−1: CFrameshift mutation
EN6Deletion422499735−1: CFrameshift mutation
DVU2402EN2SNP962507986G → AArg → Cys
DVU2405EN5SNP812510695C → AGlu → STOP
EN11Deletion1002510695−1: CFrameshift mutation
SNP1002510695C → TGlu → Lys
Table 4

Newly acquired mutations in nitrogen regulatory protein C family (NRC) genes in the EN populations.

GenePopulationsMutation typeAllele frequency (%)Mutation positionNucleotide changeAmino-acid change
DVU2394EN3Deletion162497229−1: G2 amino acids changed
SNP592497736C → TGlu → Lys
EN5SNP162496979T → CTyr → Cys
EN6Deletion492497411−1: GFrameshift mutation
EN7Deletion1002497258−18: GCAATTCACGCACGTTGC6 amino acids loss
EN9Deletion362497708−19:GAACAGTTCGCTACGGGCCFrameshift mutation
Insertion112497728+12: GACCGCGGACAT4 amino acids inserted
DVU2395EN4Deletion1002499096−8: CGGCGAGCFrameshift mutation
EN8Insertion462498544+2: CG4 amino acids changed
262499078+14:CCTCATGCGCCACCFrameshift mutation
EN9Deletion542499384−1: TFrameshift mutation
EN10SNP152498363T → CSilent mutation
SNP232498737T → CLys → Glu
SNP452498935G → AGln → STOP
EN12SNP1002499244G → AGln → STOP
DVU2396EN1SNP202499926G → APro → Ser
SNP722500012G → TSer → STOP
EN2Deletion982499984−1: CFrameshift mutation
EN6Deletion422499735−1: CFrameshift mutation
DVU2402EN2SNP962507986G → AArg → Cys
DVU2405EN5SNP812510695C → AGlu → STOP
EN11Deletion1002510695−1: CFrameshift mutation
SNP1002510695C → TGlu → Lys
GenePopulationsMutation typeAllele frequency (%)Mutation positionNucleotide changeAmino-acid change
DVU2394EN3Deletion162497229−1: G2 amino acids changed
SNP592497736C → TGlu → Lys
EN5SNP162496979T → CTyr → Cys
EN6Deletion492497411−1: GFrameshift mutation
EN7Deletion1002497258−18: GCAATTCACGCACGTTGC6 amino acids loss
EN9Deletion362497708−19:GAACAGTTCGCTACGGGCCFrameshift mutation
Insertion112497728+12: GACCGCGGACAT4 amino acids inserted
DVU2395EN4Deletion1002499096−8: CGGCGAGCFrameshift mutation
EN8Insertion462498544+2: CG4 amino acids changed
262499078+14:CCTCATGCGCCACCFrameshift mutation
EN9Deletion542499384−1: TFrameshift mutation
EN10SNP152498363T → CSilent mutation
SNP232498737T → CLys → Glu
SNP452498935G → AGln → STOP
EN12SNP1002499244G → AGln → STOP
DVU2396EN1SNP202499926G → APro → Ser
SNP722500012G → TSer → STOP
EN2Deletion982499984−1: CFrameshift mutation
EN6Deletion422499735−1: CFrameshift mutation
DVU2402EN2SNP962507986G → AArg → Cys
DVU2405EN5SNP812510695C → AGlu → STOP
EN11Deletion1002510695−1: CFrameshift mutation
SNP1002510695C → TGlu → Lys
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