Transcript #00000203

Transcript name transcript variant 4
Gene name NDUFS1 (NADH dehydrogenase (ubiquinone) Fe-S protein 1, 75kDa (NADH-coenzyme Q reductase))
Chromosome 2
Transcript - NCBI ID NM_001199983.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001186912.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

64 entries on 1 page. Showing entries 1 - 64.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-126C>G p.(=) - - - -
./. - - c.-19+1110C>T p.(=) - - - -
./. - - c.-19+1169C>T p.(=) - - - -
./. - - c.-18-10_-18-9del p.(=) - - - -
./. - - c.91-15del p.(=) - - - -
./. - - c.91-15_91-14insT p.(=) - - - -
./. - - c.193G>A p.(Ala65Thr) - - - -
./. - - c.225C>A p.(Asp75Glu) - - - -
./. - - c.243T>C p.(=) - - - -
./. - - c.250-7A>G p.(=) - - - -
./. - - c.380+14C>A p.(=) - - - -
./. - - c.495_497del p.(Ile166del) - - - -
+/+ - - c.495_497del p.(Ile166del) - - - -
./. - 7/18 c.508C>T p.(Pro170Ser) probably_damaging(0.998) missense_variant - deleterious(0)
./. - - c.512T>C p.(Val171Ala) - - - -
+/+ - 7/18 c.520C>G p.(Leu174Val) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.520C>G p.(Leu174Val) - - - -
+/+ - 7/18 c.550C>T p.(Arg184Trp) probably_damaging(0.995) missense_variant - deleterious(0)
./. - - c.550C>T p.(Arg184Trp) - - - -
./. - - c.566+1G>A p.? - - - -
+/+ - 8/18 c.584A>G p.(Asp195Gly) probably_damaging(1) missense_variant - deleterious(0.03)
./. - - c.584A>G p.(Asp195Gly) - - - -
./. - - c.587T>G p.(Val196Gly) - - - -
./. - - c.674A>G p.(Asn225Ser) - - - -
./. - - c.737C>G p.(Thr246Ser) - - - -
./. - - c.795G>T p.(=) - - - -
./. - - c.804C>T p.(=) - - - -
./. - - c.949A>G p.(Thr317Ala) - - - -
./. - - c.1051C>T p.(Arg351Cys) - - - -
+/+ - 11/18 c.1051C>T p.(Arg351Cys) possibly_damaging(0.691) missense_variant - deleterious(0)
./. - - c.1078A>G p.(Arg360Gly) - - - -
./. - - c.1080A>G p.(=) - - - -
./. - - c.1120C>G p.(Leu374Val) - - - -
./. - - c.1192A>G p.(Ile398Val) - - - -
./. - - c.1200G>A p.(=) - - - -
./. - - c.1222-7del p.(=) - - - -
./. - - c.1345G>A p.(Val449Ile) - - - -
./. - - c.1383-1G>A p.? - - - -
+/+ - 14/18 c.1498C>T p.(Arg500*) - stop_gained - -
./. - - c.1498C>T p.(Arg500*) - - - -
+/+ - 15/18 c.1612A>G p.(Thr538Ala) probably_damaging(0.92) missense_variant - deleterious(0.03)
./. - - c.1612A>G p.(Thr538Ala) - - - -
+/+ - 15/18 c.1684G>A p.(Asp562Asn) probably_damaging(1) missense_variant - tolerated(0.13)
./. - - c.1684G>A p.(Asp562Asn) - - - -
./. - - c.1835A>G p.(Asn612Ser) - - - -
./. - - c.1958G>A p.(Cys653Tyr) - - - -
./. - - c.*27C>T p.(=) - - - -
./. - - c.*93_*94insA p.(=) - - - -
./. - - c.*151T>C p.(=) - - - -
./. - - c.*158T>C p.(=) - - - -
./. - - c.*256C>T p.(=) - - - -
./. - - c.*336G>T p.(=) - - - -
./. - - c.*399G>A p.(=) - - - -
./. - - c.*438C>T p.(=) - - - -
./. - - c.*457T>A p.(=) - - - -
./. - - c.*504G>A p.(=) - - - -
./. - - c.*561T>C p.(=) - - - -
./. - - c.*641A>G p.(=) - - - -
./. - - c.*733A>G p.(=) - - - -
./. - - c.*756A>T p.(=) - - - -
./. - - c.*846del p.(=) - - - -
./. - - c.*846_*847insT p.(=) - - - -
./. - - c.*866A>C p.(=) - - - -
./. - - c.*966A>G p.(=) - - - -
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