Transcript #00021908 (NM_206945.3, TRPM3 gene)

Transcript name transcript variant 4
Gene name TRPM3 (transient receptor potential cation channel, subfamily M, member 3)
Chromosome 9
Transcript - NCBI ID NM_206945.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_996828.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-577975C>T r.(?) p.(=)
-?/. - c.-463189_-463188insTC r.(?) p.(=)
-?/. - c.-463185_-463181del r.(?) p.(=)
?/. - c.-252649G>T r.(?) p.(=)
?/. - c.-252493_-252490del r.(?) p.(=)
?/. - c.-252470T>G r.(?) p.(=)
-?/. - c.-282-15dup r.(=) p.(=)
-/. - c.-282-9C>T r.(=) p.(=)
?/. - c.-282G>A r.(?) p.(=)
-?/. - c.-282G>A r.(?) p.(=)
?/. - c.-179G>T r.(?) p.(=)
?/. - c.-83C>T r.(?) p.(=)
?/. - c.175A>G r.(?) p.(Met59Val)
-?/. - c.218-8_218-7insA r.(=) p.(=)
-/. - c.218-4_218-3dup r.spl? p.?
?/. - c.218-2A>T r.spl? p.?
?/. - c.268C>T r.(?) p.(Arg90Ter)
-?/. i c.514+16613G>A r.(=) p.(=)
-/. - c.514+17769A>C r.(=) p.(=)
+?/. - c.514+17799C>T r.(=) p.(=)
+?/. - c.514+17799C>T r.(=) p.(=)
+?/. - c.514+17799C>T r.(=) p.(=)
+?/. - c.514+17799C>T r.(=) p.(=)
+?/. - c.514+17799C>T r.(=) p.(=)
+?/. - c.514+17799C>T r.(=) p.(=)
?/. - c.674A>G r.(?) p.(Tyr225Cys)
?/. - c.904C>G r.(?) p.(Pro302Ala)
?/. - c.949G>A r.(?) p.(Ala317Thr)
?/. - c.953G>A r.(?) p.(Arg318His)
?/. - c.1054C>T r.(?) p.(Leu352Phe)
-?/. - c.1082G>A r.(?) p.(Arg361His)
?/. - c.1133C>T r.(?) p.(Pro378Leu)
?/. - c.1351-876_1351-873del r.(=) p.(=)
?/. - c.1352A>T r.(?) p.(Asp451Val)
-?/. - c.1370G>A r.(?) p.(Arg457Gln)
-?/. - c.1370G>A r.(?) p.(Arg457Gln)
?/. - c.1550T>G r.(?) p.(Val517Gly)
-?/. - c.1719G>A r.(?) p.(Thr573=)
-?/. - c.1782C>T r.(?) p.(=)
-?/. - c.1791C>T r.(?) p.(Ile597=)
?/. - c.1862G>T r.(?) p.(Gly621Val)
?/. - c.1868A>G r.(?) p.(Lys623Arg)
-?/. - c.1869+6G>A r.(=) p.(=)
?/. - c.2038G>A r.(?) p.(Ala680Thr)
-?/. - c.2064G>C r.(?) p.(Glu688Asp)
-?/. - c.2178+10T>C r.(=) p.(=)
?/. - c.2510T>C r.(?) p.(Phe837Ser)
+/. - c.2515G>A r.(?) p.(Val839Met)
+/. - c.2515G>A r.(?) p.(Val839Met)
+?/. 20 c.2515G>A r.(?) p.(Val839Met)
-?/. - c.2535G>A r.(?) p.(Pro845=)
?/. - c.2572A>T r.(?) p.(Met858Leu)
?/. - c.2759G>A r.(?) p.(Arg920Gln)
?/. - c.2816C>T r.(?) p.(Pro939Leu)
?/. - c.3007A>G r.(?) p.(Met1003Val)
?/. - c.3042G>A r.(?) p.(Trp1014*)
-/. - c.3086-7dup r.(=) p.(=)
?/. - c.3086-7dup r.(=) p.(=)
-?/. - c.3100G>A r.(?) p.(Asp1034Asn)
?/. - c.3328G>A r.(?) p.(Gly1110Arg)
-?/. - c.3478C>A r.(?) p.(Leu1160Ile)
?/. - c.3603G>T r.(?) p.(Lys1201Asn)
?/. - c.3664G>A r.(?) p.(Val1222Ile)
-?/. - c.3807C>T r.(?) p.(Ser1269=)
-?/. - c.3819T>C r.(?) p.(Leu1273=)
?/. - c.3917G>A r.(?) p.(Arg1306Gln)
-?/. - c.4039C>T r.(?) p.(Arg1347Cys)
?/. - c.4088_4089del r.(?) p.(Glu1363Glyfs*8)
?/. - c.4244C>T r.(?) p.(Ala1415Val)
?/. - c.4360C>T r.(?) p.(Arg1454Cys)
?/. - c.4537C>T r.(?) p.(Arg1513Trp)
?/. - c.4580C>T r.(?) p.(Ser1527Phe)
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