Transcript #00000127

Transcript name transcript variant X2
Gene name FARS2 (phenylalanyl-tRNA synthetase 2, mitochondrial)
Chromosome 6
Transcript - NCBI ID XM_005248812.1
Transcript - Ensembl ID -
Protein - NCBI ID XP_005248869.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

82 entries on 1 page. Showing entries 1 - 82.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.21G>T p.(Arg7Ser) - - - -
./. - - c.28G>T p.(Ala10Ser) - - - -
./. - - c.101C>T p.(Ser34Leu) - - - -
./. - - c.102G>A p.(=) - - - -
./. - - c.170C>G p.(Ser57Cys) - - - -
./. - - c.183C>T p.(=) - - - -
./. - - c.192C>G p.(Ser64Arg) - - - -
./. - - c.253C>G p.(Pro85Ala) - - - -
./. - - c.310C>T p.(Arg104Cys) - - - -
./. - - c.324G>A p.(=) - - - -
./. - - c.332C>T p.(Ser111Leu) - - - -
./. - - c.339C>T p.(=) - - - -
./. - - c.344A>G p.(Asn115Ser) - - - -
./. - - c.354A>G p.(=) - - - -
./. - - c.390C>A p.(=) - - - -
./. - - c.403C>G p.(His135Asp) - - - -
./. - - c.407C>A p.(Pro136His) - - - -
./. - - c.411C>A p.(Ser137Arg) - - - -
./. - - c.426C>A p.(Asp142Glu) - - - -
+/+ - 2/7 c.431A>G p.(Tyr144Cys) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.431A>G p.(Tyr144Cys) - - - -
./. - - c.457A>G p.(Arg153Gly) - - - -
./. - - c.462G>T p.(=) - - - -
./. - - c.467C>T p.(Thr156Met) - - - -
./. - - c.468G>A p.(=) - - - -
./. - - c.476A>C p.(His159Pro) - - - -
./. - - c.497C>T p.(Ala166Val) - - - -
./. - - c.506A>T p.(Asp169Val) - - - -
./. - - c.530T>A p.(Val177Asp) - - - -
./. - - c.550G>A p.(Asp184Asn) - - - -
./. - - c.563A>G p.(Tyr188Cys) - - - -
./. - - c.578A>G p.(Gln193Arg) - - - -
./. - - c.585G>A p.(=) - - - -
./. - - c.606G>A p.(=) - - - -
./. - - c.613-11T>C p.(=) - - - -
./. - - c.613-4A>G p.? - - - -
./. - - c.638A>G p.(Glu213Gly) - - - -
./. - - c.667C>T p.(Arg223Cys) - - - -
./. - - c.676C>T p.(His226Tyr) - - - -
./. - - c.706G>A p.(Val236Met) - - - -
./. - - c.730A>C p.(Lys244Gln) - - - -
./. - - c.737C>T p.(Thr246Met) - - - -
./. - - c.748C>T p.(Leu250Phe) - - - -
./. - - c.750C>A p.(=) - - - -
./. - - c.754G>A p.(Ala252Thr) - - - -
./. - - c.768A>C p.(=) - - - -
./. - - c.781A>T p.(Ile261Leu) - - - -
./. - - c.792del p.(Asp265Thrfs*29) - - - -
./. - - c.819T>A p.(=) - - - -
./. - - c.839A>C p.(Asn280Thr) - - - -
./. - - c.839A>G p.(Asn280Ser) - - - -
./. - - c.873C>T p.(=) - - - -
./. - - c.905-1G>A p.? - - - -
./. - - c.919C>T p.(Arg307*) - - - -
./. - - c.925G>A p.(Gly309Ser) - - - -
./. - - c.971A>G p.(Tyr324Cys) - - - -
./. - - c.973G>T p.(Asp325Tyr) - - - -
./. - - c.984T>C p.(=) - - - -
+/+ - 5/7 c.986T>C p.(Ile329Thr) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.986T>C p.(Ile329Thr) - - - -
./. - - c.1009G>A p.(Glu337Lys) - - - -
./. - - c.1014C>T p.(=) - - - -
./. - - c.1054G>T p.(Val352Leu) - - - -
./. - - c.1066-15C>G p.(=) - - - -
./. - - c.1069C>T p.(Leu357Phe) - - - -
./. - - c.1082C>T p.(Pro361Leu) - - - -
./. - - c.1083G>A p.(=) - - - -
./. - - c.1094A>G p.(Asn365Ser) - - - -
./. - - c.1109_1111delinsAACCAGAATGAA p.(Trp370*) - - - -
./. - - c.1145A>G p.(Tyr382Cys) - - - -
./. - - c.1156C>G p.(Arg386Gly) - - - -
./. - - c.1163T>G p.(Ile388Ser) - - - -
./. - - c.1172A>T p.(Asp391Val) - - - -
+/+ - 6/7 c.1172A>T p.(Asp391Val) probably_damaging(0.997) missense_variant - deleterious(0)
./. - - c.1209A>G p.(=) - - - -
./. - - c.1220C>T p.(Thr407Met) - - - -
./. - - c.1267C>T p.(Arg423Trp) - - - -
./. - - c.1268G>A p.(Arg423Gln) - - - -
./. - - c.1296C>T p.(=) - - - -
./. - - c.1308C>G p.(=) - - - -
./. - - c.1344G>A p.(=) - - - -
./. - - c.*4C>T p.(=) - - - -
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