Transcript #00001153

Transcript name transcript variant X1
Gene name SLC25A15 (solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15)
Chromosome 13
Transcript - NCBI ID XM_005266210.1
Transcript - Ensembl ID -
Protein - NCBI ID XP_005266267.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

87 entries on 1 page. Showing entries 1 - 87.
Legend  

Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
+/+ - 2/6 c.40G>A p.(Gly14Arg) - missense_variant - -
./. - - c.40G>A p.(Gly14Arg) - - - -
./. - - c.56C>G p.(Thr19Arg) - - - -
+/+ - 2/6 c.56C>G p.(Thr19Arg) - missense_variant - -
./. - - c.71T>G p.(Met24Arg) - - - -
+/+ - 2/6 c.71T>G p.(Met24Arg) - missense_variant - -
./. - - c.78G>A p.(=) - - - -
./. - - c.143G>A p.(Arg48His) - - - -
+/+ - 2/6 c.173T>A p.(Leu58Gln) - missense_variant - -
./. - - c.173T>A p.(Leu58Gln) - - - -
./. - - c.186C>T p.(=) - - - -
./. - - c.239G>A p.(Arg80Gln) - - - -
./. - - c.294C>T p.(=) - - - -
+/+ - 3/6 c.298G>A p.(Gly100Ser) - missense_variant - -
+/+ - 3/6 c.298G>T p.(Gly100Cys) - missense_variant - -
./. - - c.298G>T p.(Gly100Cys) - - - -
./. - - c.304T>G p.(Phe102Val) - - - -
./. - - c.306C>T p.(=) - - - -
./. - - c.341C>T p.(Thr114Met) - - - -
./. - - c.407del p.(Ser136Thrfs*45) - - - -
./. - - c.496C>T p.(Arg166*) - - - -
+/+ - 4/6 c.496C>T p.(Arg166*) - stop_gained - -
+/+ - 4/6 c.499G>A p.(Glu167Lys) - missense_variant - -
./. - - c.499G>A p.(Glu167Lys) - - - -
./. - - c.513T>C p.(=) - - - -
./. - - c.514_516del p.(Phe175del) - - - -
+?/+? - - c.514_516del p.(Phe175del) - - - -
./. - - c.523_525del p.(Phe175del) - - - -
./. - - c.523_525del p.(Phe175del) - - - -
+/+ - 4/6 c.525C>G p.(Phe175Leu) - missense_variant - -
./. - - c.525C>G p.(Phe175Leu) - - - -
+/+ - 4/6 c.525C>T p.(=) - synonymous_variant - -
./. - - c.526G>A p.(Gly176Ser) - - - -
+/+ - 4/6 c.530G>A p.(Gly177Asp) - missense_variant - -
./. - - c.530G>A p.(Gly177Asp) - - - -
./. - - c.593C>T p.(Pro198Leu) - - - -
./. - - c.619G>A p.(Gly207Arg) - - - -
+/+ - 5/6 c.619G>A p.(Gly207Arg) - missense_variant - -
./. - - c.721A>T p.(Ile241Leu) - - - -
./. - - c.750G>A p.(=) - - - -
+/+ - 6/6 c.776C>T p.(Thr259Ile) - missense_variant - -
./. - - c.776C>T p.(Thr259Ile) - - - -
./. - - c.779T>A p.(Met260Lys) - - - -
+/+ - 6/6 c.779T>A p.(Met260Lys) - missense_variant - -
+/+ - 6/6 c.784C>T p.(Arg262*) - stop_gained - -
./. - - c.784C>T p.(Arg262*) - - - -
./. - - c.785G>A p.(Arg262Gln) - - - -
+/+ - 6/6 c.785G>A p.(Arg262Gln) - missense_variant - -
./. - - c.808C>T p.(Leu270Phe) - - - -
+/+ - 6/6 c.808C>T p.(Leu270Phe) - missense_variant - -
./. - - c.*48T>A p.(=) - - - -
./. - - c.*58G>T p.(=) - - - -
./. - - c.*159C>G p.(=) - - - -
./. - - c.*217G>A p.(=) - - - -
./. - - c.*353A>G p.(=) - - - -
./. - - c.*420T>G p.(=) - - - -
./. - - c.*515A>G p.(=) - - - -
./. - - c.*579C>T p.(=) - - - -
./. - - c.*610G>T p.(=) - - - -
./. - - c.*639G>A p.(=) - - - -
./. - - c.*640C>T p.(=) - - - -
./. - - c.*684C>T p.(=) - - - -
./. - - c.*871T>C p.(=) - - - -
./. - - c.*898C>T p.(=) - - - -
./. - - c.*929G>C p.(=) - - - -
./. - - c.*1319G>C p.(=) - - - -
./. - - c.*1345G>C p.(=) - - - -
./. - - c.*1485T>A p.(=) - - - -
./. - - c.*1494A>G p.(=) - - - -
./. - - c.*1595G>A p.(=) - - - -
./. - - c.*1626A>G p.(=) - - - -
./. - - c.*1641G>T p.(=) - - - -
./. - - c.*1682C>T p.(=) - - - -
./. - - c.*1721C>T p.(=) - - - -
./. - - c.*1737G>A p.(=) - - - -
./. - - c.*1829_*1833del p.(=) - - - -
./. - - c.*1855C>A p.(=) - - - -
./. - - c.*1945G>A p.(=) - - - -
./. - - c.*1982A>C p.(=) - - - -
./. - - c.*2071C>T p.(=) - - - -
./. - - c.*2097T>A p.(=) - - - -
./. - - c.*2105A>T p.(=) - - - -
./. - - c.*2190T>C p.(=) - - - -
./. - - c.*2264C>T p.(=) - - - -
./. - - c.*2328G>T p.(=) - - - -
./. - - c.*2373T>C p.(=) - - - -
./. - - c.*2494G>A p.(=) - - - -
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