Transcript #00025340 (NM_032034.3, SLC4A11 gene)

Transcript name transcript variant 2
Gene name SLC4A11 (solute carrier family 4, sodium borate transporter, member 11)
Chromosome 20
Transcript - NCBI ID NM_032034.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_114423.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2018-11-13 13:26:46 +01:00 (CET)
Date last edited N/A


Variants

157 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.-1456G>C r.(?) p.(=)
?/. - c.-385A>G r.(?) p.(=)
-?/. - c.-273C>G r.(?) p.(=)
+?/+? ? c.? r.(=) p.(=)
+/+ ? c.? r.(?) p.(?)
+/+ ? c.? r.(=) p.(=)
-?/. - c.19C>T r.(?) p.(Arg7Trp)
?/. - c.47A>C r.(?) p.(Gln16Pro)
+/+ ? c.99_100del r.(?) p.(Pro34Hisfs*17)
?/. - c.109T>C r.(?) p.(Ser37Pro)
?/. - c.109T>C r.(?) p.(Ser37Pro)
-?/? ? c.215A>C r.(?) p.(Asn72Thr)
-?/. - c.245G>T r.(?) p.(Arg82Leu)
-?/-? ? c.271A>G r.(?) p.(Met91Val)
-?/. - c.287C>G r.(?) p.(Thr96Ser)
?/. - c.290-5G>A r.spl? p.?
+/+ ? c.353_356del r.(?) p.(Lys118Thrfs*12)
+/+ 4 c.353_356del r.(?) p.(Lys118Thrfs*12)
-?/. - c.362A>G r.(?) p.(Lys121Arg)
+/+ ? c.374G>A r.(?) p.(Arg125His)
?/. - c.377C>T r.(?) p.(Ala126Val)
-/. - c.405G>A r.(=) p.(=)
-/. - c.405G>A r.(=) p.(=)
?/. - c.409G>T r.(?) p.(Ala137Ser)
+/. - c.427G>A r.(?) p.(Glu143Lys)
+/+ 4 c.427G>A r.(?) p.(Glu143Lys)
?/. - c.427G>C r.(?) p.(Glu143Gln)
?/. - c.457C>T r.(?) p.(Arg153Trp)
-?/. - c.470G>A r.(?) p.(Arg157His)
+/+ ? c.473_480del r.(?) p.(Arg158Glnfs*4)
+/+ 4 c.473_480del r.(?) p.(Arg158Glnfs*4)
+/+ ? c.473_481delinsC r.(?) p.(Arg158Profs*4)
+/+ ? c.478G>A r.(?) p.(Ala160Thr)
-/. - c.481A>C r.(?) p.(Arg161=)
+/+ ? c.501G>C r.(?) p.(Glu167Asp)
?/. - c.501G>C r.(?) p.(Glu167Asp)
?/. - c.563G>A r.(?) p.(Arg188Gln)
+/. - c.637T>C r.(?) p.(Ser213Pro)
+/+ 5 c.637T>C r.(?) p.(Ser213Pro)
+/+ ? c.654-97_777+478del r.(=) p.(Cys219Lysfs*49)
-?/. - c.661A>G r.(?) p.(Met221Val)
+/+ ? c.695G>A r.(?) p.(Ser232Asn)
?/. - c.712C>T r.(?) p.(Gln238*)
?/? 6 c.719G>C r.(?) p.W240S
+?/. - c.777+1G>T r.spl? p.?
?/. - c.797T>C r.(?) p.(Met266Thr)
+/+ ? c.806C>T r.(?) p.(Ala269Val)
+/+ ? c.806C>T r.(?) p.(Ala269Val)
+/+ ? c.812C>T r.(?) p.(Thr271Met)
+/+ ? c.845G>C r.(?) p.(Arg282Pro)
?/. - c.950C>T r.(?) p.(Thr317Met)
-/- ? c.980C>T r.(?) p.(Ala327Val)
+/+ ? c.985A>T r.(?) p.(Arg329*)
-?/. - c.1039C>T r.(?) p.(Arg347Trp)
-?/. - c.1051G>A r.(?) p.(Ala351Thr)
-/. - c.1091-15A>C r.(=) p.(=)
-?/. - c.1091-10C>T r.(=) p.(=)
+/+ ? c.1156T>C r.(?) p.(Cys386Arg)
+/+ ? c.1156T>C r.(?) p.(Cys386Arg)
+/+ 9 c.1180G>C r.(?) p.(Gly394Arg)
+/+ ? c.1195G>A r.(?) p.(Glu399Lys)
+?/. - c.1216+1G>A r.spl p.?
-?/. - c.1216+2T>G r.spl? p.?
-?/. - c.1216+4A>G r.spl? p.?
+?/. - c.1237G>A r.(?) p.(Gly413Arg)
+/+ 10 c.1253G>A r.(?) p.(Gly418Asp)
?/? 10 c.1304C>T r.(?) p.Thr434Ile
?/. - c.1331-10del r.(=) p.(=)
?/. - c.1362G>A r.(?) p.(=)
+/+ ? c.1378_1381delinsA r.(?) p.(Tyr460_Ala461delinsThr)
+/+ 11 c.1391G>A r.(?) p.(Gly464Asp)
+/+ 11 c.1391G>A r.(?) p.(Gly464Asp)
+/+ 11 c.1391G>A r.(?) p.(Gly464Asp)
?/. - c.1421A>T r.(?) p.(Tyr474Phe)
+/+ ? c.1463G>A r.(?) p.(Arg488Lys)
+/+ 12 c.1466C>T r.(?) p.(Ser489Leu)
?/? 12 c.1519G>A r.(?) p.Val507Ile
+/+ ? c.1577A>G r.(?) p.(Tyr526Cys)
-?/. - c.1613C>T r.(?) p.(Ser538Leu)
-/. - c.1620C>T r.(?) p.(Leu540=)
-/- ? c.1682C>T r.(?) p.(Thr561Met)
-?/. - c.1682C>T r.(?) p.(Thr561Met)
-?/. - c.1683G>A r.(?) p.(Thr561=)
-?/? ? c.1694C>T r.(?) p.(Ser565Leu)
?/. - c.1694C>T r.(?) p.(Ser565Leu)
+/+ ? c.1723G>A r.(?) p.(Val575Met)
?/. - c.1741A>G r.(?) p.(Met581Val)
+/+ ? c.1748G>A r.(?) p.(Gly583Asp)
-?/. - c.1770C>G r.(?) p.(Thr590=)
+/+ ? c.1813C>T r.(?) p.(Arg605*)
+/+ 14 c.1813C>T r.(?) p.(Arg605*)
-?/. - c.1827C>T r.(?) p.(Ser609=)
-?/. - c.1833C>T r.(?) p.(Cys611=)
+/+ ? c.1850-6delinsGCCGGCCGG r.(=) p.(=)
+/+ ? c.1850-6delinsGGCCGGCCGG r.(=) p.(=)
-?/. - c.1938G>A r.(?) p.(Ala646=)
-?/. - c.1992C>T r.(?) p.(Leu664=)
+?/. - c.2003T>C r.(?) p.(Leu668Pro)
-?/. - c.2040C>T r.(?) p.(Ala680=)
-?/. - c.2058G>A r.(?) p.(Pro686=)
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