Transcript #00001220 (NM_000339.2, SLC12A3 gene)

Transcript name transcript variant 1
Gene name SLC12A3 (solute carrier family 12 (sodium/chloride transporters), member 3)
Chromosome 16
Transcript - NCBI ID NM_000339.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000330.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:19:24 +02:00 (CEST)
Date last edited N/A


Variants

469 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 25i_26_ c.(2951+1_2952-1)_*2445{0} r.? p.?
+/. 25i_26_ c.(2951+1_2952-1)_*2445{0} r.? p.?
+/. - c.1A>G r.(?) p.(Ala2_Met53del)
+/. - c.3G>A r.(?) p.(Ala2_Met53del)
?/. - c.17C>T r.(?) p.(Thr6Ile)
-?/. - c.27G>A r.(?) p.(Thr9=)
+/. - c.35dup r.(?) p.(Asp12GlufsTer18)
-/. - c.36C>T r.(?) p.(Asp12=)
-?/. - c.36C>T r.(?) p.(Asp12=)
-?/. - c.36C>T r.(?) p.(Asp12=)
+?/. - c.71C>T r.(?) p.(Thr24Ile)
?/. - c.81C>G r.(?) p.(Ser27Arg)
+/. - c.139del r.(?) p.(His47Thrfs*67)
+?/. - c.160C>T r.(?) p.(Arg54Cys)
+/. - c.179C>T r.(?) p.(Thr60Met)
+/. - c.179C>T r.(?) p.(Thr60Met)
+?/. - c.179C>T r.(?) p.(Thr60Met)
+?/. - c.184G>A r.(?) p.(Asp62Asn)
+/. - c.201T>A r.(?) p.(Tyr67Ter)
+/. - c.237_238dup r.(?) p.(Arg80ProfsTer35)
+/. - c.237_238dup r.(?) p.(Arg80ProfsTer35)
+/. - c.247C>T r.(?) p.(Arg83Trp)
+/. - c.247C>T r.(?) p.(Arg83Trp)
+/. - c.247C>T r.(?) p.(Arg83Trp)
+/. - c.247C>T r.(?) p.(Arg83Trp)
+?/. - c.247C>T r.(?) p.(Arg83Trp)
-?/. - c.249G>T r.(?) p.(Arg83=)
-/. - c.282+79T>G r.(=) p.(=)
+/. 1i c.283-438_283-387dup r.[282_283ins283-385_283-74,282_283ins283-385_283-95] p.?
+?/. - c.283-435_283-384dup r.[(282_283ins283-385_283-74,282_283ins283-385_283-95)] p.?
?/. - c.322C>T r.(?) p.(Arg108Trp)
-?/. - c.323G>A r.(?) p.(Arg108Gln)
?/. - c.334G>C r.(?) p.(Glu112Gln)
-?/. - c.363G>C r.(?) p.(Glu121Asp)
-/. - c.363G>C r.(?) p.(Glu121Asp)
-/. - c.366A>G r.(?) p.(Ala122=)
-/. - c.366A>G r.(?) p.(Ala122=)
+?/. - c.403C>T r.(?) p.(Arg135Cys)
+/. - c.429+1_429+28del r.spl p.?
-?/. - c.429+9G>A r.(=) p.(=)
-?/. - c.430-472_430-461del r.= p.=
-/. 2i c.430-472_430-461del r.= p.=
+?/. - c.457G>A r.(?) p.(Val153Met)
+?/. - c.463C>T r.(?) p.(Leu155Phe)
+?/. - c.468C>A r.(?) p.(Tyr156*)
+/. - c.473G>A r.(?) p.(Arg158Gln)
+?/. - c.473G>A r.(?) p.(Arg158Gln)
?/. - c.488C>T r.(?) p.(Thr163Met)
?/. - c.505G>T r.(?) p.(Val169Phe)
-/. - c.506-316C>T r.(=) p.(=)
+/. - c.506-1G>A r.spl? p.?
+/. - c.514T>C r.(?) p.(Trp172Arg)
+?/. - c.514T>C r.(?) p.(Trp172Arg)
+?/. - c.514T>C r.(?) p.(Trp172Arg)
+/. - c.514T>C r.(?) p.(Trp172Arg)
+/. - c.533C>T r.(?) p.(Ser178Leu)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+/. - c.539C>A r.(?) p.(Thr180Lys)
+?/. - c.539C>A r.(?) p.(Thr180Lys)
+?/. - c.557G>A r.(?) p.(Gly186Asp)
+/. - c.601+1G>A r.spl? p.?
+?/. - c.602-16G>A r.(=) p.(=)
+/. - c.602-16G>A r.[(601_621ins602-14_601-1,601_602ins[601+1_602-17;a;602-15_602-1])] p.(Ser200_Gly201insAlaLeuPro*)
+/. - c.602-16G>A r.[(601_621ins602-14_601-1,601_602ins[601+1_602-17;a;602-15_602-1])] p.(Ser200_Gly201insAlaLeuPro*)
+/. 4i c.602-16G>A r.[601_621ins602-14_601-1,601_602ins[601+1_602-17;a;602-15_602-1]] p.?
+?/. - c.602-11T>A r.[(601_621ins602-9_601-1,601_602ins[601+1_602-11;a;602-9_602-1])] p.(Ser200_Gly201insAlaLeuIle)
+/. 4i c.602-11T>A r.[601_621ins602-9_601-1,601_602ins[601+1_602-11;a;602-9_602-1]] p.?
+?/. - c.602G>T r.(?) p.(Gly201Val)
+/. - c.625C>T r.(?) p.(Arg209Trp)
+?/. - c.625C>T r.(?) p.(Arg209Trp)
+/. - c.644T>C r.(?) p.(Leu215Pro)
+?/. - c.644T>C r.(?) p.(Leu215Pro)
+/. - c.644T>C r.(?) p.(Leu215Pro)
-?/. - c.651C>T r.(?) p.(Gly217=)
+?/. - c.671C>A r.(?) p.(Ala224Asp)
?/. - c.676G>A r.(?) p.(Ala226Thr)
?/. - c.698T>C r.(?) p.(Met233Thr)
?/. - c.704C>T r.(?) p.(Thr235Met)
?/. - c.727C>T r.(?) p.(Arg243Trp)
+/. - c.741+1G>A r.spl? p.?
+?/. - c.741+1G>A r.spl? p.?
-?/. - c.741+9G>A r.(=) p.(=)
-?/. - c.774C>T r.(?) p.(Asn258=)
+/. - c.788_805dup r.(?) p.(Ile263_Val268dup)
-/. - c.791= r.(=) p.(Gly264=)
-/. - c.791= r.(=) p.(Gly264=)
-/. - c.791C>G r.(?) p.(Ala264Gly)
-/. - c.791C>G r.(?) p.(Ala264Gly)
?/. - c.791G>A r.(?) p.(Gly264Asp)
+/. - c.815T>C r.(?) p.(Leu272Pro)
+?/. - c.815T>C r.(?) p.(Leu272Pro)
+?/. - c.815T>C r.(?) p.(Leu272Pro)
-?/. - c.852+7_852+9del r.(=) p.(=)
+?/. - c.852+243C>T r.[(852_853ins852+121_852+241,=)] p.?
+?/. - c.852+243C>T r.[(852_853ins852+121_852+241,=)] p.?
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