Transcript #00001145

Transcript name solute carrier family 22 (organic cation/carnitine transporter), member 5
Gene name SLC22A5 (solute carrier family 22 (organic cation/carnitine transporter), member 5)
Chromosome 5
Transcript - NCBI ID NM_003060.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003051.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

394 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-207C>G p.(=) - - - -
+?/+? - - c.-185C>A p.(=) - - - -
./. - - c.-149G>A p.(=) - - - -
+/+ - - c.-149G>A p.(=) - - - -
./. - - c.-139G>T p.(=) - - - -
./. - - c.-131A>C p.(=) - - - -
./. - - c.-130_-103del p.(=) - - - -
./. - - c.-118G>A p.(=) - - - -
./. - - c.-107G>T p.(=) - - - -
./. - - c.-91_8del p.? - - - -
+/+ - - c.-91_22del p.? - - - -
-/- - - c.-78C>T p.(=) - - - -
./. - - c.-78C>T p.(=) - - - -
./. - - c.-77G>A p.(=) - - - -
-/- - - c.-77G>A p.(=) - - - -
-/- - - c.-38C>A p.(=) - - - -
./. - - c.-30G>C p.(=) - - - -
./. - - c.-25C>T p.(=) - - - -
./. - - c.1A>G p.? - - - -
./. - - c.1A>T p.? - - - -
./. - - c.2T>G p.? - - - -
+/+ - 1/10 c.3G>T p.? possibly_damaging(0.742) initiator_codon_variant - tolerated(0.06)
./. - - c.3G>T p.? - - - -
./. - - c.3_4insC p.(Arg2Profs*136) - - - -
./. - 1/10 c.3_4insC p.(Arg2Profs*136) - frameshift_variant - -
?/? - 1/10 c.3_4insC p.(Arg2Profs*136) - frameshift_variant - -
?/? - - c.4dup p.(Arg2Profs*136) - - - -
./. - 1/10 c.4_5insCG p.(Arg2Profs*7) - frameshift_variant - -
./. - - c.12C>G p.(Tyr4*) - - - -
+/+ - 1/10 c.12C>G p.(Tyr4*) - stop_gained - -
./. - - c.13del p.(Asp5Thrfs*3) - - - -
+/+ - 1/10 c.34G>A p.(Gly12Ser) probably_damaging(0.997) missense_variant - deleterious(0)
./. - - c.34G>A p.(Gly12Ser) - - - -
./. - - c.39G>C p.(Glu13Asp) - - - -
./. - - c.40T>A p.(Trp14Arg) - - - -
./. - - c.40_41insGGG p.(Gly15dup) - - - -
./. - - c.43G>T p.(Gly15Trp) - - - -
+/+ - 1/10 c.43G>T p.(Gly15Trp) probably_damaging(0.999) missense_variant - deleterious(0)
+/+ - 1/10 c.51C>G p.(Phe17Leu) possibly_damaging(0.703) missense_variant - deleterious(0.01)
./. - - c.51C>G p.(Phe17Leu) - - - -
./. - - c.51del p.(Gln18Serfs*25) - - - -
./. - - c.56G>C p.(Arg19Pro) - - - -
+/+ - 1/10 c.56G>C p.(Arg19Pro) possibly_damaging(0.818) missense_variant - tolerated(0.14)
+/+ - 1/10 c.59T>A p.(Leu20His) benign(0.092) missense_variant - tolerated(0.19)
./. - - c.59T>A p.(Leu20His) - - - -
./. - - c.62_64del p.(Phe23del) - - - -
+?/+? - - c.64_66del p.(Phe23del) - - - -
?/? - - c.67_69del p.(Phe23del) - - - -
./. - - c.71del p.(Leu24Argfs*19) - - - -
./. - - c.75C>T p.(=) - - - -
+/+ - 1/10 c.83G>T p.(Ser28Ile) benign(0.254) missense_variant - tolerated(0.06)
./. - - c.83G>T p.(Ser28Ile) - - - -
./. - - c.93C>T p.(=) - - - -
./. - - c.95A>G p.(Asn32Ser) - - - -
+/+ - 1/10 c.95A>G p.(Asn32Ser) benign(0.041) missense_variant - tolerated(0.05)
./. - - c.119T>A p.(Val40Glu) - - - -
./. - - c.122T>G p.(Phe41Cys) - - - -
./. - - c.131C>T p.(Ala44Val) - - - -
./. - - c.133A>G p.(Thr45Ala) - - - -
./. - - c.134del p.(Pro46Argfs*13) - - - -
+/+ - 1/10 c.136C>G p.(Pro46Ala) probably_damaging(0.992) missense_variant - deleterious(0)
./. - - c.136C>G p.(Pro46Ala) - - - -
./. - - c.136C>T p.(Pro46Ser) - - - -
+/+ - 1/10 c.136C>T p.(Pro46Ser) probably_damaging(0.992) missense_variant - deleterious(0)
+/+ - 1/10 c.137C>T p.(Pro46Leu) possibly_damaging(0.812) missense_variant - deleterious(0)
./. - - c.137C>T p.(Pro46Leu) - - - -
+/+ - - c.148del p.(Cys50Alafs*9) - - - -
./. - - c.148del p.(Cys50Alafs*9) - - - -
./. - - c.155_156insGCCGGAC p.(Ala56Glyfs*84) - - - -
./. - - c.185G>A p.(Trp62*) - - - -
-/- - 1/10 c.207G>C p.(=) - synonymous_variant - -
./. - - c.207G>C p.(=) - - - -
./. - - c.208C>T p.(Arg70Trp) - - - -
+/+ - - c.232del p.(His79Thrfs*51) - - - -
./. - - c.232del p.(His79Thrfs*51) - - - -
./. - - c.242G>A p.(Cys81Tyr) - - - -
./. - - c.246C>T p.(=) - - - -
-/- - 1/10 c.246C>T p.(=) - synonymous_variant - -
./. - - c.247C>T p.(Arg83Cys) - - - -
+/+ - 1/10 c.248G>T p.(Arg83Leu) possibly_damaging(0.708) missense_variant - deleterious(0)
./. - - c.248G>T p.(Arg83Leu) - - - -
./. - - c.250_251insACCGGCTCGCC p.(Ile89Glyfs*45) - - - -
./. - - c.250_251insACCGGCTCGCCACC p.(Ile89Thrfs*46) - - - -
./. - - c.252C>G p.(Tyr84*) - - - -
./. - 1/10 c.253_254insGGCTCGCCACC p.(Ile89Glyfs*45) - frameshift_variant - -
?/? - 1/10 c.253_254insGGCTCGCCACC p.(Ile89Glyfs*45) - frameshift_variant - -
?/? - - c.264_265insGGCTCGCCACC p.(Ile89Glyfs*45) - - - -
./. - - c.265A>G p.(Ile89Val) - - - -
./. - - c.265_266insGGCTCGCCACC p.(Ile89Argfs*45) - - - -
+/+ - 1/10 c.265_266insGGCTCGCCACC p.(Ile89Argfs*45) - frameshift_variant - -
./. - 1/10 c.265_266insGGCTCGCCACC p.(Ile89Argfs*45) - frameshift_variant - -
./. - - c.272A>G p.(Asn91Ser) - - - -
+/+ - 1/10 c.278C>G p.(Ser93Trp) probably_damaging(0.999) missense_variant - deleterious(0)
./. - - c.278C>G p.(Ser93Trp) - - - -
./. - - c.279G>C p.(=) - - - -
./. - - c.283C>G p.(Leu95Val) - - - -
+/+ - 1/10 c.283C>G p.(Leu95Val) benign(0.41) missense_variant - tolerated(0.34)
./. - - c.285T>C p.(=) - - - -
+/+ - 1/10 c.287G>C p.(Gly96Ala) probably_damaging(0.984) missense_variant - deleterious(0.01)
./. - - c.287G>C p.(Gly96Ala) - - - -
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