Transcript #00000658

Transcript name transcript variant 2
Gene name CPS1 (carbamoyl-phosphate synthase 1, mitochondrial)
Chromosome 2
Transcript - NCBI ID NM_001875.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001866.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

207 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-128G>A p.(=) - - - -
./. - - c.-76A>G p.(=) - - - -
./. - - c.-29T>G p.(=) - - - -
./. - - c.-6_-5insTCT p.(=) - - - -
./. - - c.-3delinsTTCC p.(=) - - - -
./. - - c.3G>T p.? - - - -
./. - - c.5C>T p.(Thr2Met) - - - -
./. - - c.25A>T p.(Lys9*) - - - -
./. - - c.126+1G>A p.? - - - -
./. - - c.130C>T p.(Gln44*) - - - -
+/+ - 4/5 c.130C>T p.(Gln44*) - stop_gained - -
./. - - c.167T>G p.(Met56Arg) - - - -
./. - - c.186C>T p.(=) - - - -
./. - - c.195C>T p.(=) - - - -
./. - - c.208_209insAAGTGGTT p.(Phe73Lysfs*80) - - - -
./. - - c.236+1G>T p.? - - - -
./. - - c.236+5G>A p.? - - - -
./. - - c.259C>T p.(Pro87Ser) - - - -
./. - - c.295C>A p.(Pro99Thr) - - - -
./. - - c.301del p.(Ile101Leufs*49) - - - -
./. - - c.302_303insTGGGAA p.(Asn103_Gly104dup) - - - -
./. - - c.303T>G p.(Ile101Met) - - - -
./. - - c.449G>A p.(Gly150Glu) - - - -
./. - - c.486T>C p.(=) - - - -
./. - - c.487G>T p.(Gly163*) - - - -
./. - - c.520C>T p.(Arg174Trp) - - - -
./. - - c.528G>A p.(=) - - - -
./. - - c.528+9A>G p.(=) - - - -
./. - - c.529-4A>T p.? - - - -
./. - - c.586A>G p.(Asn196Asp) - - - -
./. - - c.593_594del p.(Asn199Phefs*4) - - - -
./. - - c.637G>A p.(Gly213Ser) - - - -
./. - - c.697C>T p.(Arg233Cys) - - - -
./. - - c.711+1G>C p.? - - - -
./. - - c.712C>T p.(Arg238*) - - - -
./. - - c.713G>A p.(Arg238Gln) - - - -
./. - - c.730del p.(Leu244*) - - - -
./. - - c.763G>T p.(Glu255*) - - - -
./. - - c.783C>T p.(=) - - - -
./. - - c.795del p.(Asn267Thrfs*8) - - - -
./. - - c.838_839insAGGTGC p.? - - - -
./. - - c.902G>A p.(Gly301Glu) - - - -
./. - - c.937A>G p.(Met313Val) - - - -
./. - - c.945C>G p.(Asn315Lys) - - - -
./. - - c.948-6C>T p.(=) - - - -
+/+ - 10/38 c.1010A>G p.(His337Arg) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.1010A>G p.(His337Arg) - - - -
./. - - c.1021T>G p.(Leu341Val) - - - -
./. - - c.1025_1027del p.(Asn343del) - - - -
./. - - c.1030A>G p.(Thr344Ala) - - - -
./. - - c.1030A>T p.(Thr344Ser) - - - -
./. - - c.1032C>T p.(=) - - - -
./. - - c.1063A>G p.(Asn355Asp) - - - -
./. - - c.1068C>G p.(=) - - - -
./. - - c.1086+1G>A p.? - - - -
./. - - c.1087-7C>T p.(=) - - - -
./. - - c.1145C>T p.(Pro382Leu) - - - -
./. - - c.1165-5T>C p.? - - - -
./. - - c.1187C>A p.(Ser396*) - - - -
./. - - c.1201G>C p.(Gly401Arg) - - - -
./. - - c.1263+5G>C p.? - - - -
./. - - c.1307G>A p.(Gly436Asp) - - - -
./. - - c.1312G>A p.(Ala438Thr) - - - -
./. - - c.1312G>C p.(Ala438Pro) - - - -
./. - - c.1320_1321insT p.(Asp442*) - - - -
./. - - c.1355T>C p.(Met452Thr) - - - -
./. - - c.1359+7G>A p.(=) - - - -
./. - - c.1411_1412insC p.(Asn472Glnfs*2) - - - -
./. - - c.1437G>A p.(=) - - - -
./. - - c.1478C>T p.(Thr493Ile) - - - -
./. - - c.1528del p.(Gly510Alafs*5) - - - -
./. - - c.1569A>G p.(=) - - - -
./. - - c.1627G>A p.(Ala543Thr) - - - -
./. - - c.1631C>T p.(Thr544Met) - - - -
+/+ - 15/38 c.1631C>T p.(Thr544Met) possibly_damaging(0.573) missense_variant - deleterious(0)
./. - - c.1648T>C p.(Phe550Leu) - - - -
./. - - c.1760G>A p.(Arg587His) - - - -
./. - - c.1774_1775insT p.(Gly594Trpfs*42) - - - -
./. - - c.1837-8A>G p.(=) - - - -
./. - - c.1864G>A p.(Val622Met) - - - -
./. - - c.1895T>G p.(Ile632Arg) - - - -
./. - - c.1912C>T p.(Arg638*) - - - -
?/? - 17/38 c.1918G>T p.(Ala640Ser) benign(0.012) missense_variant - tolerated(0.14)
./. - - c.1926del p.(Asp642Glufs*39) - - - -
./. - - c.1982-8A>T p.(=) - - - -
./. - - c.1982-1G>C p.? - - - -
./. - - c.2148T>A p.(Asn716Lys) - - - -
./. - - c.2161C>T p.(Arg721*) - - - -
./. - - c.2192+6A>T p.(=) - - - -
./. - - c.2193-15G>T p.(=) - - - -
./. - - c.2193-1G>T p.? - - - -
./. - - c.2225del p.(Leu743*) - - - -
./. - - c.2265C>A p.(=) - - - -
./. - - c.2265C>T p.(=) - - - -
+/+ - 19/38 c.2359C>T p.(Arg787*) - stop_gained - -
./. - - c.2359C>T p.(Arg787*) - - - -
./. - - c.2376G>C p.(Met792Ile) - - - -
./. - - c.2391+1G>A p.? - - - -
./. - - c.2392-1G>T p.? - - - -
./. - - c.2394C>A p.(=) - - - -
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