Transcript #00000331

Transcript name transcript variant 1
Gene name TK2 (thymidine kinase 2, mitochondrial)
Chromosome 16
Transcript - NCBI ID NM_004614.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004605.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

125 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.-216G>A p.(=) - - - -
./. - - c.-48G>A p.(=) - - - -
./. - - c.-38A>G p.(=) - - - -
./. - - c.-30C>G p.(=) - - - -
./. - - c.8_9insT p.(Trp4Valfs*40) - - - -
./. - - c.8_9insT p.(Trp4Valfs*40) - - - -
+/+ - - c.8_9insT p.(Trp4Valfs*40) - - - -
./. - - c.94C>T p.(Arg32Trp) - - - -
./. - - c.122C>A p.(Pro41His) - - - -
./. - - c.124+6G>C p.(=) - - - -
./. - - c.129_132del p.(Lys43Asnfs*9) - - - -
+/+ - - c.129_132del p.(Lys43Asnfs*9) - - - -
+/+ - 2/9 c.133C>T p.(Gln45*) - stop_gained - -
./. - - c.133C>T p.(Gln45*) - - - -
./. - - c.142_143insG p.(Glu48Glyfs*102) - - - -
+/+ - - c.142_143insG p.(Glu48Glyfs*102) - - - -
./. - - c.142_143insG p.(Glu48Glyfs*102) - - - -
./. - - c.150_151insA p.(Ser51Ilefs*99) - - - -
./. - - c.150_151insA p.(Ser51Ilefs*99) - - - -
+/+ - - c.150_151insA p.(Ser51Ilefs*99) - - - -
./. - - c.156+2T>C p.? - - - -
+/+ - - c.156+2T>C p.? - splice_donor_variant - -
./. - - c.156+15T>C p.(=) - - - -
./. - - c.156+1208del p.(=) - - - -
./. - - c.157-12G>A p.(=) - - - -
./. - - c.159C>G p.(Ile53Met) - - - -
+/+ - 3/10 c.159C>G p.(Ile53Met) possibly_damaging(0.863) missense_variant,splice_region_variant - deleterious(0)
./. - - c.173A>G p.(Asn58Ser) - - - -
+/+ - 3/10 c.173A>G p.(Asn58Ser) probably_damaging(0.998) missense_variant - deleterious(0)
+/+ - 3/10 c.191C>T p.(Thr64Met) probably_damaging(0.978) missense_variant - deleterious(0)
./. - - c.191C>T p.(Thr64Met) - - - -
./. - - c.198C>G p.(Cys66Trp) - - - -
+/+ - 3/10 c.198C>G p.(Cys66Trp) probably_damaging(0.984) missense_variant - tolerated(0.16)
./. - 3/10 c.198C>T p.(=) - synonymous_variant - -
./. - 3/10 c.218_219insCG p.(Thr74Glyfs*7) - frameshift_variant - -
./. - - c.219_220insCG p.(Thr74Argfs*7) - - - -
+/+ - - c.219_220insCG p.(Thr74Argfs*7) - - - -
./. - - c.219_220insCG p.(Thr74Argfs*7) - - - -
./. - - c.231+10C>T p.(=) - - - -
./. - - c.268C>T p.(Arg90Cys) - - - -
+/+ - 4/10 c.268C>T p.(Arg90Cys) benign(0.021) missense_variant - tolerated(0.07)
+/+ - 4/10 c.278A>G p.(Asn93Ser) possibly_damaging(0.45) missense_variant - deleterious(0.01)
./. - - c.278A>G p.(Asn93Ser) - - - -
./. - - c.288C>T p.(=) - - - -
+/+ - 5/10 c.323C>T p.(Thr108Met) probably_damaging(0.97) missense_variant - tolerated(0.09)
./. - - c.323C>T p.(Thr108Met) - - - -
./. - - c.334T>A p.(Tyr112Asn) - - - -
+/+ - 5/10 c.334T>A p.(Tyr112Asn) probably_damaging(0.966) missense_variant - deleterious(0)
./. - 5/10 c.335_336insAT p.(Tyr112*) - stop_gained,frameshift_variant - -
./. - - c.336_337insAT p.(Val113Metfs*20) - - - -
./. - - c.336_337insAT p.(Val113Metfs*20) - - - -
+/+ - - c.336_337insAT p.(Val113Metfs*20) - - - -
./. - - c.360_361delinsAA p.(His121Asn) - - - -
+/+ - - c.360_361delinsAA p.(His121Asn) - - - -
./. - - c.361C>A p.(His121Asn) - - - -
+/+ - 5/10 c.361C>A p.(His121Asn) probably_damaging(0.976) missense_variant - deleterious(0)
+/+ - 5/10 c.373C>T p.(Gln125*) - stop_gained,splice_region_variant - -
./. - - c.373C>T p.(Gln125*) - - - -
./. - - c.388C>T p.(Arg130Trp) - - - -
+/+ - 6/10 c.388C>T p.(Arg130Trp) probably_damaging(0.999) missense_variant - deleterious(0)
+/+ - 6/10 c.389G>A p.(Arg130Gln) probably_damaging(0.971) missense_variant - deleterious(0.02)
./. - - c.389G>A p.(Arg130Gln) - - - -
+/+ - 6/10 c.416C>T p.(Ala139Val) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.416C>T p.(Ala139Val) - - - -
./. - - c.450-13A>G p.(=) - - - -
./. - 8/10 c.547C>A p.(=) - synonymous_variant - -
./. - - c.547C>G p.(Arg183Gly) - - - -
./. - 8/10 c.547C>G p.(Arg183Gly) possibly_damaging(0.844) missense_variant - deleterious(0)
./. - - c.547C>T p.(Arg183Trp) - - - -
+/+ - 8/10 c.547C>T p.(Arg183Trp) probably_damaging(0.967) missense_variant - deleterious(0)
+/+ - 8/10 c.562A>G p.(Thr188Ala) benign(0.057) missense_variant - tolerated(0.15)
./. - - c.562A>G p.(Thr188Ala) - - - -
./. - - c.575G>A p.(Arg192Lys) - - - -
+/+ - 8/10 c.575G>A p.(Arg192Lys) probably_damaging(0.996) missense_variant - deleterious(0.01)
./. - - c.604_606del p.(Lys202del) - - - -
+/+ - - c.604_606del p.(Lys202del) - - - -
+/+ - 9/10 c.635T>A p.(Ile212Asn) probably_damaging(0.954) missense_variant - deleterious(0)
./. - - c.635T>A p.(Ile212Asn) - - - -
+/+ - 9/10 c.644T>C p.(Leu215Pro) probably_damaging(0.988) missense_variant - deleterious(0.01)
./. - - c.644T>C p.(Leu215Pro) - - - -
./. - - c.680C>T p.(Pro227Leu) - - - -
./. - - c.699+6_699+9del p.(=) - - - -
./. - - c.700-13G>A p.(=) - - - -
./. - - c.760C>T p.(Arg254*) - - - -
+/+ - 10/10 c.760C>T p.(Arg254*) - stop_gained - -
./. - - c.*342C>A p.(=) - - - -
./. - - c.*444G>T p.(=) - - - -
./. - - c.*451G>A p.(=) - - - -
./. - - c.*485C>G p.(=) - - - -
./. - - c.*595G>A p.(=) - - - -
./. - - c.*615A>C p.(=) - - - -
./. - - c.*688C>T p.(=) - - - -
./. - - c.*765T>C p.(=) - - - -
./. - - c.*809C>T p.(=) - - - -
./. - - c.*833T>G p.(=) - - - -
./. - - c.*921G>A p.(=) - - - -
./. - - c.*1044C>A p.(=) - - - -
./. - - c.*1333G>T p.(=) - - - -
./. - - c.*1403A>G p.(=) - - - -
./. - - c.*1443C>A p.(=) - - - -
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