Transcript #00000329

Transcript name transcript variant 3
Gene name TK2 (thymidine kinase 2, mitochondrial)
Chromosome 16
Transcript - NCBI ID NM_001172644.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001166115.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

119 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.94C>T p.(Arg32Trp) - - - -
./. - - c.122C>A p.(Pro41His) - - - -
./. - - c.124+6G>C p.(=) - - - -
./. - - c.129_132del p.(Lys43Asnfs*11) - - - -
+/+ - - c.129_132del p.(Lys43Asnfs*11) - - - -
+/+ - 2/9 c.133C>T p.(Gln45*) - stop_gained - -
./. - - c.133C>T p.(Gln45*) - - - -
./. - - c.142_143insG p.(Glu48Glyfs*77) - - - -
./. - - c.142_143insG p.(Glu48Glyfs*77) - - - -
./. - - c.150_151insA p.(Ser51Ilefs*74) - - - -
./. - - c.150_151insA p.(Ser51Ilefs*74) - - - -
+/+ - - c.156+2T>C p.? - splice_donor_variant - -
./. - - c.156+2T>C p.? - - - -
./. - - c.156+15T>C p.(=) - - - -
./. - - c.157-4948G>A p.(=) - - - -
+/+ - - c.157-4934C>G p.(=) - - - -
./. - - c.157-4934C>G p.(=) - - - -
+/+ - - c.157-4920A>G p.(=) - - - -
./. - - c.157-4920A>G p.(=) - - - -
+/+ - - c.157-4902C>T p.(=) - - - -
./. - - c.157-4902C>T p.(=) - - - -
./. - - c.157-4895C>G p.(=) - - - -
+/+ - - c.157-4895C>G p.(=) - - - -
./. - - c.157-4895C>T p.(=) - - - -
./. - - c.157-4875_157-4874insCG p.(=) - - - -
./. - - c.157-4874_157-4873insCG p.(=) - - - -
./. - - c.157-4874_157-4873insCG p.(=) - - - -
./. - - c.157-4852C>T p.(=) - - - -
+/+ - 3/9 c.193C>T p.(Arg65Cys) benign(0.014) missense_variant - tolerated(0.06)
./. - - c.193C>T p.(Arg65Cys) - - - -
+/+ - 3/9 c.203A>G p.(Asn68Ser) benign(0.256) missense_variant - deleterious(0.01)
./. - - c.203A>G p.(Asn68Ser) - - - -
./. - - c.213C>T p.(=) - - - -
./. - - c.248C>T p.(Thr83Met) - - - -
+/+ - 4/9 c.248C>T p.(Thr83Met) probably_damaging(0.978) missense_variant - tolerated(0.08)
./. - - c.259T>A p.(Tyr87Asn) - - - -
+/+ - 4/9 c.259T>A p.(Tyr87Asn) probably_damaging(0.996) missense_variant - deleterious(0)
./. - 4/9 c.260_261insAT p.(Tyr87*) - stop_gained,frameshift_variant - -
./. - - c.261_262insAT p.(Val88Metfs*20) - - - -
./. - - c.261_262insAT p.(Val88Metfs*20) - - - -
./. - - c.285_286delinsAA p.(His96Asn) - - - -
+/+ - - c.285_286delinsAA p.(His96Asn) - - - -
+/+ - 4/9 c.286C>A p.(His96Asn) probably_damaging(0.92) missense_variant - deleterious(0)
./. - - c.286C>A p.(His96Asn) - - - -
./. - - c.298C>T p.(Gln100*) - - - -
+/+ - 4/9 c.298C>T p.(Gln100*) - stop_gained,splice_region_variant - -
+/+ - 5/9 c.313C>T p.(Arg105Trp) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.313C>T p.(Arg105Trp) - - - -
./. - - c.314G>A p.(Arg105Gln) - - - -
+/+ - 5/9 c.314G>A p.(Arg105Gln) probably_damaging(0.984) missense_variant - tolerated(0.1)
+/+ - 5/9 c.341C>T p.(Ala114Val) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.341C>T p.(Ala114Val) - - - -
./. - - c.375-13A>G p.(=) - - - -
./. - 7/9 c.472C>A p.(=) - synonymous_variant - -
./. - 7/9 c.472C>G p.(Arg158Gly) possibly_damaging(0.836) missense_variant - deleterious(0)
./. - - c.472C>G p.(Arg158Gly) - - - -
./. - - c.472C>T p.(Arg158Trp) - - - -
+/+ - 7/9 c.472C>T p.(Arg158Trp) probably_damaging(0.949) missense_variant - deleterious(0)
./. - - c.487A>G p.(Thr163Ala) - - - -
+/+ - 7/9 c.487A>G p.(Thr163Ala) benign(0.057) missense_variant - tolerated(0.1)
+/+ - 7/9 c.500G>A p.(Arg167Lys) probably_damaging(0.994) missense_variant - deleterious(0.01)
./. - - c.500G>A p.(Arg167Lys) - - - -
./. - - c.529_531del p.(Lys177del) - - - -
+/+ - - c.529_531del p.(Lys177del) - - - -
+/+ - 8/9 c.560T>A p.(Ile187Asn) probably_damaging(0.971) missense_variant - deleterious(0)
./. - - c.560T>A p.(Ile187Asn) - - - -
./. - - c.569T>C p.(Leu190Pro) - - - -
+/+ - 8/9 c.569T>C p.(Leu190Pro) probably_damaging(0.995) missense_variant - deleterious(0.01)
./. - - c.605C>T p.(Pro202Leu) - - - -
./. - - c.624+6_624+9del p.(=) - - - -
./. - - c.625-13G>A p.(=) - - - -
+/+ - 9/9 c.685C>T p.(Arg229*) - stop_gained - -
./. - - c.685C>T p.(Arg229*) - - - -
./. - - 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.(=) - - - -
./. - - c.*1455C>G p.(=) - - - -
./. - - c.*1472A>T p.(=) - - - -
./. - - c.*1591_*1592insT p.(=) - - - -
./. - - c.*1618C>A p.(=) - - - -
./. - - c.*1681A>G p.(=) - - - -
./. - - c.*1682T>G p.(=) - - - -
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