Transcript #00000243

Transcript name transcript variant 3
Gene name PC (pyruvate carboxylase)
Chromosome 11
Transcript - NCBI ID NM_001040716.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001035806.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

126 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-282G>A p.(=) - - - -
./. - - c.-274A>C p.(=) - - - -
./. - - c.1-35661G>T p.(=) - - - -
./. - - c.52C>A p.(=) - - - -
./. - - c.52C>T p.(Arg18*) - - - -
./. - - c.75C>T p.(=) - - - -
./. - 5/23 c.184C>T p.(Arg62Cys) probably_damaging(0.953) missense_variant - deleterious(0)
./. - - c.184C>T p.(Arg62Cys) - - - -
+/+ - 5/23 c.184C>T p.(Arg62Cys) probably_damaging(0.953) missense_variant - deleterious(0)
./. - - c.216G>A p.(=) - - - -
./. - - c.227A>T p.(His76Leu) - - - -
-/- - 5/23 c.227A>T p.(His76Leu) probably_damaging(0.982) missense_variant - deleterious(0)
./. - - c.331G>A p.(Val111Ile) - - - -
./. - - c.372_375del p.(Ala125Thrfs*79) - - - -
./. - - c.434T>C p.(Val145Ala) - - - -
./. - 6/23 c.434T>C p.(Val145Ala) benign(0.084) missense_variant - tolerated(0.42)
+/+ - 6/23 c.434T>C p.(Val145Ala) benign(0.084) missense_variant - tolerated(0.42)
./. - - c.467G>A p.(Arg156Gln) - - - -
./. - 6/23 c.467G>A p.(Arg156Gln) probably_damaging(0.957) missense_variant - deleterious(0)
+/+ - 6/23 c.467G>A p.(Arg156Gln) probably_damaging(0.957) missense_variant - deleterious(0)
./. - - c.496G>A p.(Val166Ile) - - - -
./. - - c.543C>T p.(=) - - - -
./. - - c.584C>T p.(Ala195Val) - - - -
./. - - c.633+2T>C p.? - - - -
./. - - c.633+38_633+58del p.(=) - - - -
./. - - c.715A>G p.(Ile239Val) - - - -
./. - - c.786G>T p.(Glu262Asp) - - - -
./. - - c.788G>A p.(Arg263Gln) - - - -
+/+ - 9/23 c.796T>A p.(Ser266Thr) probably_damaging(0.951) missense_variant - deleterious(0.02)
./. - - c.796T>A p.(Ser266Thr) - - - -
./. - 9/23 c.796T>A p.(Ser266Thr) probably_damaging(0.951) missense_variant - deleterious(0.02)
./. - - c.796T>G p.(Ser266Ala) - - - -
./. - - c.806G>A p.(Arg269Gln) - - - -
./. - - c.879C>T p.(=) - - - -
./. - - c.927C>T p.(=) - - - -
./. - - c.1022+1G>A p.? - - - -
./. - - c.1023-14C>G p.(=) - - - -
./. - - c.1054G>T p.(Ala352Ser) - - - -
-/- - 11/23 c.1054G>T p.(Ala352Ser) possibly_damaging(0.702) missense_variant - deleterious(0.02)
./. - - c.1167G>A p.(=) - - - -
./. - - c.1181T>C p.(Ile394Thr) - - - -
./. - - c.1185+5_1185+8del p.? - - - -
./. - - c.1225_1227del p.(Asn409del) - - - -
./. - - c.1233C>T p.(=) - - - -
./. - - c.1344G>A p.(=) - - - -
+/+ - 11/22 c.1351C>T p.(Arg451Cys) probably_damaging(0.982) missense_variant - deleterious(0)
./. - 11/22 c.1351C>T p.(Arg451Cys) probably_damaging(0.982) missense_variant - deleterious(0)
./. - - c.1351C>T p.(Arg451Cys) - - - -
./. - - c.1357C>T p.(Arg453*) - - - -
./. - - c.1368+1G>A p.? - - - -
./. - - c.1401C>T p.(=) - - - -
./. - - c.1513+9C>A p.(=) - - - -
./. - - c.1513+13del p.(=) - - - -
./. - - c.1514-6C>T p.(=) - - - -
./. - - c.1608G>A p.(=) - - - -
./. - - c.1646G>A p.(Gly549Glu) - - - -
./. - - c.1702A>G p.(Thr568Ala) - - - -
./. - - c.1705A>G p.(Thr569Ala) - - - -
+/+ - 14/22 c.1705A>G p.(Thr569Ala) possibly_damaging(0.676) missense_variant - deleterious(0)
./. - 14/22 c.1705A>G p.(Thr569Ala) possibly_damaging(0.676) missense_variant - deleterious(0)
+/+ - 14/22 c.1748G>T p.(Arg583Leu) probably_damaging(1) missense_variant - deleterious(0)
./. - 14/22 c.1748G>T p.(Arg583Leu) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.1748G>T p.(Arg583Leu) - - - -
./. - - c.1825+1G>A p.? - - - -
./. - 16/23 c.1828G>A p.(Ala610Thr) probably_damaging(1) missense_variant,splice_region_variant - deleterious(0)
./. - - c.1828G>A p.(Ala610Thr) - - - -
+/+ - 16/23 c.1828G>A p.(Ala610Thr) probably_damaging(1) missense_variant,splice_region_variant - deleterious(0)
./. - - c.1832C>T p.(Thr611Met) - - - -
./. - - c.1892G>A p.(Arg631Gln) - - - -
+/+ - 16/23 c.1892G>A p.(Arg631Gln) probably_damaging(1) missense_variant - deleterious(0)
./. - 16/23 c.1892G>A p.(Arg631Gln) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.2095G>A p.(Val699Met) - - - -
./. - - c.2095G>T p.(Val699Leu) - - - -
+/+ - 16/22 c.2114C>A p.(Ser705*) - stop_gained - -
./. - 16/22 c.2114C>A p.(Ser705*) - stop_gained - -
./. - - c.2114C>A p.(Ser705*) - - - -
./. - - c.2224-15_2224-14del p.(=) - - - -
./. - - c.2224-9T>G p.(=) - - - -
./. - - c.2229G>T p.(Met743Ile) - - - -
+/+ - 17/22 c.2229G>T p.(Met743Ile) probably_damaging(0.976) missense_variant - deleterious(0)
./. - 17/22 c.2229G>T p.(Met743Ile) probably_damaging(0.976) missense_variant - deleterious(0)
./. - - c.2286C>G p.(=) - - - -
-/- - 17/22 c.2286C>G p.(=) - synonymous_variant - -
./. - 17/22 c.2286C>T p.(=) - synonymous_variant - -
./. - - c.2292C>G p.(=) - - - -
./. - - c.2493_2494del p.(Phe832*) - - - -
./. - - c.2540C>T p.(Ala847Val) - - - -
+/+ - 18/22 c.2540C>T p.(Ala847Val) benign(0.145) missense_variant - tolerated(0.09)
./. - 18/22 c.2540C>T p.(Ala847Val) benign(0.145) missense_variant - tolerated(0.09)
./. - - c.2550C>T p.(=) - - - -
./. - - c.2580C>T p.(=) - - - -
./. - - c.2606G>A p.(Gly869Asp) - - - -
./. - - c.2610_2611insGGCCAG p.(Gly869_Gln870dup) - - - -
-/- - 18/22 c.2619C>T p.(=) - synonymous_variant - -
./. - - c.2619C>T p.(=) - - - -
./. - - c.2668G>T p.(Val890Phe) - - - -
./. - - c.2705G>A p.(Gly902Asp) - - - -
./. - - c.2714_2716del p.(Ile905del) - - - -
./. - - c.2719-5_2719-3del p.? - - - -
./. - - c.2723C>T p.(Thr908Met) - - - -
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