Transcript #00000180

Transcript name mitochondrial translation optimization 1 homolog (S. cerevisiae), transcript variant 2
Gene name MTO1 (mitochondrial tRNA translation optimization 1)
Chromosome 6
Transcript - NCBI ID NM_012123.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_036255.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

52 entries on 1 page. Showing entries 1 - 52.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.61C>T p.(Pro21Ser) - - - -
./. - - c.70C>T p.(Arg24Trp) - - - -
./. - - c.176G>C p.(Gly59Ala) - - - -
./. - - c.252C>T p.(=) - - - -
./. - - c.547A>G p.(Thr183Ala) - - - -
./. - - c.620C>T p.(Thr207Met) - - - -
./. - - c.623A>G p.(His208Arg) - - - -
./. - - c.919G>A p.(Glu307Lys) - - - -
./. - - c.922A>G p.(Thr308Ala) - - - -
./. - - c.938G>A p.(Arg313Gln) - - - -
./. - - c.963A>C p.(Lys321Asn) - - - -
./. - - c.983G>A p.(Arg328His) - - - -
./. - - c.1051A>G p.(Met351Val) - - - -
./. - - c.1062A>C p.(=) - - - -
./. - - c.1082T>C p.(Met361Thr) - - - -
./. - - c.1086C>G p.(Ile362Met) - - - -
./. - - c.1134C>T p.(=) - - - -
./. - - c.1194G>T p.(Leu398Phe) - - - -
./. - - c.1222A>G p.(Ile408Val) - - - -
+/+ - 7/13 c.1232C>T p.(Thr411Ile) probably_damaging(0.966) missense_variant - deleterious(0)
./. - - c.1232C>T p.(Thr411Ile) - - - -
./. - - c.1260+191G>A p.(=) - - - -
./. - - c.1260+193C>A p.(=) - - - -
./. - - c.1260+238C>T p.(=) - - - -
./. - - c.1260+288G>A p.(=) - - - -
./. - - c.1261-5T>G p.? - - - -
./. - - c.1282G>A p.(Ala428Thr) - - - -
+/+ - 8/12 c.1282G>A p.(Ala428Thr) probably_damaging(0.977) missense_variant - deleterious(0)
./. - - c.1291C>T p.(Arg431Trp) - - - -
./. - - c.1339A>G p.(Ile447Val) - - - -
./. - - c.1368T>C p.(=) - - - -
./. - - c.1429C>T p.(Arg477Cys) - - - -
./. - - c.1430G>A p.(Arg477His) - - - -
+/+ - 8/12 c.1430G>A p.(Arg477His) probably_damaging(0.987) missense_variant - deleterious(0)
./. - - c.1450C>T p.(Arg484Trp) - - - -
./. - - c.1480G>A p.(Gly494Ser) - - - -
./. - - c.1549G>A p.(Val517Met) - - - -
./. - - c.1717A>T p.(Thr573Ser) - - - -
./. - - c.1785A>G p.(=) - - - -
?/? - 11/12 c.1813_1814insA p.(Asp605Glufs*2) - frameshift_variant - -
./. - - c.1822del p.(Leu608Serfs*7) - - - -
./. - - c.1827A>G p.(=) - - - -
./. - - c.1857_1858insA p.(Arg620Lysfs*8) - - - -
?/? - 11/12 c.1857_1858insA p.(Arg620Lysfs*8) - frameshift_variant - -
./. - - c.1894C>T p.(=) - - - -
./. - - c.1918-7T>G p.(=) - - - -
./. - - c.1934G>A p.(Arg645His) - - - -
./. - - c.1940C>T p.(Pro647Leu) - - - -
./. - - c.1956C>T p.(=) - - - -
./. - - c.1996C>T p.(Arg666*) - - - -
./. - - c.2036A>G p.(Gln679Arg) - - - -
./. - - c.2064A>G p.(=) - - - -
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