Transcript #00024238 (NM_152989.3, SOX5 gene)

Transcript name transcript variant 2
Gene name SOX5 (SRY (sex determining region Y)-box 5)
Chromosome 12
Transcript - NCBI ID NM_152989.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_694534.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-03-05 20:07:06 +01:00 (CET)
Date last edited N/A


Variants

100 entries on 1 page. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 12i_18_ c.(1125+1_1304-1178)_*1922{0} r.? p.?
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
?/. _1_3i c.-374_(-98-25322_-98-1)del r.0 p.0?
?/. 1i_3i c.(-258+1_-257-26374)_(-99+6139_-98-1)del r.0 p.0?
-/. - c.-99+1del r.spl? p.?
-?/. - c.-99+1del r.spl? p.?
-?/. - c.-98-40648G>A r.(=) p.(=)
-?/. - c.-2+25300C>A r.(=) p.(=)
+/. 4i c.(-2+1_-2+64582)_(-1-61559_-1-53679)del r.? p.0?
+/. 3i_4i c.(-2+1_-2+80171)_(-1-46427_232-1)del r.? p.0?
+/. 4i_18_ c.(-2+1_-1-90871)_(*1922_?)del r.? p.0?
-?/. - c.-1-53624C>T r.(=) p.(=)
+/. 10i_18_ c.(892+1_892+10598)_*1922{0} r.? p.?
+/. 11i_18_ c.(978+1_979-1)_*1922{0} r.? p.?
+/. _1_6i c.-374_(443-16074_443-1){0} r.0? p.0?
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. _1_18_ c.-374_*1922{0} r.0 p.0
+/. 14i c.-374_*1922{1} r.? p.?
+/. 14i c.-374_*1922{1} r.? p.?
+/. _1_18_ c.-374_*1922{1} r.0 p.0
?/. - c.16C>G r.(?) p.(Pro6Ala)
-?/. - c.26C>T r.(?) p.(Pro9Leu)
-?/. - c.26C>T r.(?) p.(Pro9Leu)
-?/. - c.76G>A r.(?) p.(Val26Met)
-?/. - c.126T>C r.(?) p.(His42=)
?/. - c.155A>G r.(?) p.(Glu52Gly)
+?/. 2 c.195T>A r.(?) p.(Cys65*)
?/. - c.206C>T r.(?) p.(Thr69Ile)
?/. - c.229A>G r.(?) p.(Met77Val)
+?/. - c.231+1del r.spl? p.?
+/. 5i_6i c.(?_231+6759)_(443-16142_?)del r.? p.?
+/. - c.253_254del r.(?) p.(Met85ValfsTer28)
?/. - c.298G>A r.(?) p.(Ala100Thr)
?/. - c.314G>A r.(?) p.(Arg105Gln)
?/. - c.433G>A r.(?) p.(Glu145Lys)
?/. - c.435G>T r.(?) p.(Glu145Asp)
-?/. - c.442+166C>T r.(=) p.(=)
+/. 5i_9i c.442+10881_771+33036del r.? p.?
+/. 5i_9i c.442+10881_771+33036del r.? p.?
-?/. - c.443-259A>C r.(=) p.(=)
+/. - c.479G>A r.(?) p.(Trp160Ter)
?/. - c.583C>T r.(?) p.(Gln195Ter)
+/. - c.598C>T r.(?) p.(Arg200*)
+?/. - c.698_699insT r.(?) p.(Glu233AspfsTer41)
-?/. - c.711A>G r.(?) p.(Arg237=)
+?/. - c.757C>T r.(?) p.(Gln253Ter)
-?/. - c.772-14762dup r.(=) p.(=)
?/. - c.824G>C r.(?) p.(Arg275Pro)
+/. - c.847C>T r.(?) p.(Gln283Ter)
+?/. 11 c.865C>T r.(?) p.(Pro289Ser)
?/. - c.889T>A r.(?) p.(Cys297Ser)
?/. - c.920C>T r.(?) p.(Pro307Leu)
?/. - c.940G>A r.(?) p.(Ala314Thr)
+/. - c.1021G>T r.(?) p.(Gly341*)
+/. - c.1059_1060del r.(?) p.(Ala354CysfsTer23)
?/. - c.1096A>G r.(?) p.(Ser366Gly)
+?/. - c.1097del r.(?) p.(Ser366Thrfs*17)
+/. - c.1168del r.(?) p.(Thr390Profs*18)
-?/. - c.1175A>T r.(?) p.(Asp392Val)
-?/. - c.1187C>A r.(?) p.(Pro396His)
?/. - c.1187C>A r.(?) p.(Pro396His)
?/. - c.1199C>T r.(?) p.(Thr400Ile)
+/. - c.1372C>T r.(?) p.(Arg458*)
?/. - c.1373G>C r.(?) p.(Arg458Pro)
+/. - c.1381C>T r.(?) p.(Gln461Ter)
+/. - c.1456dup r.(?) p.(Thr486AsnfsTer13)
?/. - c.1497G>C r.(?) p.(Gln499His)
?/. - c.1528A>G r.(?) p.(Met510Val)
+/. - c.1558+5G>A r.spl? p.?
?/. - c.1596A>C r.(?) p.(Glu532Asp)
+/. - c.1600C>T r.(?) p.(Arg534Ter)
+/. - c.1600C>T r.(?) p.(Arg534Ter)
+?/. - c.1634G>A r.(?) p.(Arg545His)
+?/. - c.1634G>A r.(?) p.(Arg545His)
+?/. - c.1634G>A r.(?) p.(Arg545His)
+?/. 13 c.1634G>C r.(?) p.(Arg545Pro)
+?/. - c.1653G>A r.(?) p.(Met551Ile)
+/. - c.1658G>A r.(?) p.(Trp553*)
?/. - c.1672C>T r.(?) p.(Arg558Trp)
?/. - c.1672C>T r.(?) p.(Arg558Trp)
?/. - c.1673G>A r.(?) p.(Arg558Gln)
+?/. - c.1673G>A r.(?) p.(Arg558Gln)
+?/. - c.1721G>A r.(?) p.(Ser574Asn)
-?/. - c.1732+9A>G r.(=) p.(=)
+?/. - c.1738C>T r.(?) p.(Arg580Cys)
+?/. - c.1739G>A r.(?) p.(Arg580His)
+?/. 17 c.1792C>G r.(?) p.(Arg598Gly)
+/. - c.1804C>T r.(?) p.(Gln602*)
+?/. - c.1822C>T r.(?) p.(Pro608Ser)
?/. - c.1823C>G r.(?) p.(Pro608Arg)
-?/. - c.1825G>A r.(?) p.(Asp609Asn)
?/. - c.1909C>T r.(?) p.(Arg637Cys)
?/. - c.2036C>T r.(?) p.(Pro679Leu)
?/. - c.2157T>A r.(?) p.(Asn719Lys)
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