Transcript #00000660

Transcript name transcript variant 2
Gene name CPT1A (carnitine palmitoyltransferase 1A (liver))
Chromosome 11
Transcript - NCBI ID NM_001031847.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001027017.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

101 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.96T>G p.(Tyr32*) - - - -
+/+ - 2/4 c.96T>G p.(Tyr32*) - stop_gained - -
./. - - c.100T>C p.(Ser34Pro) - - - -
./. - - c.186G>A p.(Trp62*) - - - -
./. - - c.200_202del p.(Val67del) - - - -
./. - - c.222C>A p.(Tyr74*) - - - -
./. - - c.281+1G>A p.? - - - -
./. - - c.282-1G>A p.? - - - -
+/+ - 4/4 c.298C>T p.(Gln100*) - stop_gained - -
./. - - c.298C>T p.(Gln100*) - - - -
+/+ - 4/4 c.367C>T p.(Arg123Cys) possibly_damaging(0.692) missense_variant - deleterious(0)
./. - - c.367C>T p.(Arg123Cys) - - - -
+/+ - 5/19 c.478C>T p.(Arg160*) - stop_gained - -
./. - - c.478C>T p.(Arg160*) - - - -
./. - - c.548_549del p.(Val183Glufs*130) - - - -
./. - - c.693+1G>C p.? - - - -
./. - - c.693+1G>T p.? - - - -
./. - - c.694-2A>G p.? - - - -
./. - - c.727C>T p.(Arg243*) - - - -
./. - - c.771+1G>C p.? - - - -
./. - - c.772-2A>G p.? - - - -
./. - - c.772-1G>A p.? - - - -
+/+ - 8/19 c.823G>A p.(Ala275Thr) benign(0.006) missense_variant - tolerated(0.38)
./. - - c.823G>A p.(Ala275Thr) - - - -
+/+ - 8/19 c.823G>C p.(Ala275Pro) possibly_damaging(0.719) missense_variant - deleterious(0.03)
+/+ - 9/19 c.912C>G p.(Cys304Trp) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.912C>G p.(Cys304Trp) - - - -
./. - - c.919C>T p.(Gln307*) - - - -
+/+ - 9/19 c.941C>T p.(Thr314Ile) probably_damaging(0.99) missense_variant - deleterious(0)
./. - - c.941C>T p.(Thr314Ile) - - - -
./. - - c.946C>G p.(Arg316Gly) - - - -
+/+ - 9/19 c.946C>G p.(Arg316Gly) probably_damaging(0.998) missense_variant - deleterious(0)
./. - - c.948del p.(Ile317Serfs*12) - - - -
+/+ - - c.948del p.(Ile317Serfs*12) - - - -
./. - - c.967+1G>A p.? - - - -
./. - - c.967+2T>C p.? - - - -
./. - - c.1027T>G p.(Phe343Val) - - - -
+/+ - 10/19 c.1027T>G p.(Phe343Val) possibly_damaging(0.711) missense_variant - deleterious(0.02)
+/+ - 10/19 c.1069C>T p.(Arg357Trp) probably_damaging(0.943) missense_variant - tolerated(0.06)
./. - - c.1069C>T p.(Arg357Trp) - - - -
./. - - c.1079A>G p.(Glu360Gly) - - - -
+/+ - 10/19 c.1079A>G p.(Glu360Gly) probably_damaging(0.973) missense_variant - deleterious(0)
./. - - c.1163+1G>A p.? - - - -
./. - - c.1163+2T>C p.? - - - -
./. - - c.1241C>T p.(Ala414Val) - - - -
+/+ - 11/19 c.1241C>T p.(Ala414Val) probably_damaging(0.984) missense_variant - deleterious(0)
./. - - c.1274_1276del p.(Glu425del) - - - -
./. - - c.1298del p.(Asp433Valfs*98) - - - -
+/+ - 11/19 c.1339C>T p.(Arg447*) - stop_gained - -
./. - - c.1339C>T p.(Arg447*) - - - -
./. - - c.1348_1352+4del p.? - - - -
./. - - c.1361A>G p.(Asp454Gly) - - - -
+/+ - 12/19 c.1361A>G p.(Asp454Gly) probably_damaging(0.928) missense_variant - deleterious(0.03)
./. - - c.1364A>C p.(Lys455Thr) - - - -
./. - - c.1367C>T p.(Ser456Leu) - - - -
./. - - c.1386del p.(Phe462Leufs*69) - - - -
./. - - c.1393G>A p.(Gly465Arg) - - - -
+/+ - 12/19 c.1393G>T p.(Gly465Trp) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.1393G>T p.(Gly465Trp) - - - -
./. - - c.1425G>A p.(Trp475*) - - - -
+/+ - 12/19 c.1425G>A p.(Trp475*) - stop_gained - -
+/+ - 12/19 c.1436C>T p.(Pro479Leu) possibly_damaging(0.479) missense_variant - deleterious(0)
./. - - c.1436C>T p.(Pro479Leu) - - - -
./. - - c.1451T>C p.(Leu484Pro) - - - -
+/+ - 12/19 c.1451T>C p.(Leu484Pro) benign(0.249) missense_variant - deleterious(0.05)
./. - - c.1458+1G>A p.? - - - -
./. - - c.1459-1G>A p.? - - - -
+/+ - 13/19 c.1493A>G p.(Tyr498Cys) probably_damaging(0.992) missense_variant - deleterious(0)
./. - - c.1493A>G p.(Tyr498Cys) - - - -
+/+ - 13/19 c.1494T>A p.(Tyr498*) - stop_gained - -
./. - - c.1494T>A p.(Tyr498*) - - - -
./. - - c.1494T>G p.(Tyr498*) - - - -
+/+ - 13/19 c.1494T>G p.(Tyr498*) - stop_gained - -
./. - - c.1575+1G>A p.? - - - -
+/+ - - c.1575+1_1575+84del p.? - - - -
./. - - c.1575+533_1575+534del p.(=) - - - -
./. - - c.1576-2A>G p.? - - - -
+/+ - - c.1600del p.(Leu534*) - - - -
./. - - c.1600del p.(Leu534*) - - - -
./. - - c.1711C>T p.(Gln571*) - - - -
./. - - c.1737C>A p.(Tyr579*) - - - -
+/+ - 14/19 c.1737C>A p.(Tyr579*) - stop_gained - -
./. - - c.1875+10_1875+33del p.(=) - - - -
./. - - c.1876-1G>A p.? - - - -
+/+ - - c.1876-1G>A p.? - splice_acceptor_variant - -
./. - - c.1876-1G>C p.? - - - -
./. - - c.1997_1998insAAAA p.(Tyr666*) - - - -
./. - - c.2027_2028+2del p.? - - - -
./. - - c.2028+2T>G p.? - - - -
./. - - c.2028+3_2028+6del p.? - - - -
+?/+? - - c.2028+3_2028+6del p.? - - - -
./. - - c.2071C>T p.(Gln691*) - - - -
./. - - c.2095_2107del p.(Leu699Glnfs*46) - - - -
./. - - c.2095_2107del p.(Leu699Glnfs*46) - - - -
./. - - c.2126G>A p.(Gly709Glu) - - - -
+/+ - 17/19 c.2126G>A p.(Gly709Glu) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.2129G>A p.(Gly710Glu) - - - -
+/+ - 17/19 c.2129G>A p.(Gly710Glu) probably_damaging(1) missense_variant - deleterious(0)
+/+ - 18/19 c.2156G>A p.(Gly719Asp) probably_damaging(0.998) missense_variant - deleterious(0)
./. - - c.2156G>A p.(Gly719Asp) - - - -
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