Transcript #00001151

Transcript name solute carrier family 25, member 13 (citrin), transcript variant 1
Gene name SLC25A13 (solute carrier family 25 (aspartate/glutamate carrier), member 13)
Chromosome 7
Transcript - NCBI ID NM_001160210.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001153682.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

53 entries on 1 page. Showing entries 1 - 53.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.15G>A p.(=) - - - -
+/+ - 1/5 c.15G>A p.(=) - splice_region_variant,synonymous_variant,NMD_transcript_variant - -
./. - - c.468+1G>C p.? - - - -
./. - - c.493C>T p.(Gln165*) - - - -
./. - - c.495del p.(Ala166Profs*30) - - - -
+/+ - 6/18 c.550C>T p.(Arg184*) - stop_gained - -
./. - - c.550C>T p.(Arg184*) - - - -
+/+ - - c.615+1G>C p.? - splice_donor_variant - -
./. - - c.615+1G>C p.? - - - -
./. - - c.615+5G>A p.? - - - -
+/+ - - c.615+5G>A p.? - - - -
./. - - c.616-11A>G p.(=) - - - -
+/+ - 7/18 c.674C>A p.(Ser225*) - stop_gained - -
./. - - c.674C>A p.(Ser225*) - - - -
./. - - c.775C>T p.(Gln259*) - - - -
./. - - c.852_855del p.(Met285Profs*2) - - - -
+/+ - - c.851_854del p.(Met285Profs*2) - - - -
./. - - c.1066C>T p.(Arg356*) - - - -
+?/+? - 11/18 c.1067G>A p.(Arg356Gln) probably_damaging(0.993) missense_variant - deleterious(0)
./. - - c.1067G>A p.(Arg356Gln) - - - -
./. - 11/18 c.1078C>T p.(Gln360*) - stop_gained - -
+/+ - 11/18 c.1081C>T p.(Arg361*) - stop_gained - -
./. - - c.1081C>T p.(Arg361*) - - - -
?/? - 11/18 c.1178G>A p.(Arg393Lys) possibly_damaging(0.792) missense_variant,splice_region_variant - tolerated(0.06)
./. - - c.1180+1G>A p.? - - - -
+/+ - - c.1180+1G>A p.? - splice_donor_variant - -
./. - - c.1270G>A p.(Asp424Asn) - - - -
./. - - c.1314C>T p.(=) - - - -
+/+ - - c.1314+1G>A p.? - splice_donor_variant - -
./. - - c.1314+1G>A p.? - - - -
./. - - c.1508C>T p.(Pro503Leu) - - - -
./. - - c.1595G>A p.(Gly532Asp) - - - -
+/+ - 16/18 c.1595G>A p.(Gly532Asp) probably_damaging(1) missense_variant,splice_region_variant - deleterious(0)
./. - - c.1663_1664insGAGATTACAGGTGGCTGCCCGGG p.(Ala555Glyfs*17) - - - -
./. - - c.1663_1664insGAGATTACAGGTGGCTGCCCGGG p.(Ala555Glyfs*17) - - - -
./. - - c.1663_1664insGAGATTACAGGTGGCTGCCCGGG p.(Ala555Glyfs*17) - - - -
./. - - c.1667_1668insAGATTACAGGTGGCTGCCCGGGG p.(Gln557Aspfs*15) - - - -
./. - - c.1766G>A p.(Arg589Gln) - - - -
+/+ - 17/18 c.1766G>A p.(Arg589Gln) probably_damaging(0.952) missense_variant - deleterious(0.01)
?/? - 17/18 c.1799_1800insA p.(Tyr601Leufs*11) - frameshift_variant - -
./. - - c.1802_1803insA p.(Tyr601*) - - - -
./. - - c.1802_1803insA p.(Tyr601*) - - - -
./. - - c.1802_1803insA p.(Tyr601*) - - - -
./. - - c.1804G>A p.(Glu602Lys) - - - -
+/+ - 17/18 c.1804G>A p.(Glu602Lys) possibly_damaging(0.581) missense_variant - deleterious(0)
+/+ - 17/18 c.1804G>T p.(Glu602*) - stop_gained - -
./. - - c.1804G>T p.(Glu602*) - - - -
./. - 17/18 c.1813C>T p.(Gln605*) - stop_gained - -
+/+ - 17/18 c.1816C>T p.(Arg606*) - stop_gained - -
./. - - c.1816C>T p.(Arg606*) - - - -
./. - - c.1913T>C p.(Val638Ala) - - - -
./. - - c.1919del p.(Gly640Alafs*61) - - - -
./. - - c.1961A>G p.(Lys654Arg) - - - -
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