Transcript #00025234 (NM_001014797.2, KCNMA1 gene)

Transcript name transcript variant 1
Gene name KCNMA1 (potassium large conductance calcium-activated channel, subfamily M, alpha member 1)
Chromosome 10
Transcript - NCBI ID NM_001014797.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001014797.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-10-23 16:16:51 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. 19 c.? r.? p.?
?/. - c.15_16insAGC r.(?) p.(Gly5_Gly6insSer)
-?/. - c.15_16insAGC r.(?) p.(Gly5_Gly6insSer)
?/. - c.27_56del r.(?) p.(Gly13_Ser22del)
?/. - c.29_30insAGG r.(?) p.(Gly10dup)
-?/. - c.31A>G r.(?) p.(Ser11Gly)
-/. - c.34A>G r.(?) p.(Ser12Gly)
-?/. - c.51_56dup r.(?) p.(Gly19_Gly20dup)
?/. - c.51_56dup r.(?) p.(Gly19_Gly20dup)
-?/. - c.54_56dup r.(?) p.(Gly20dup)
-?/. - c.54_56dup r.(?) p.(Gly20dup)
?/. - c.54_56dup r.(?) p.(Gly20dup)
?/. - c.71G>A r.(?) p.(Arg24Lys)
?/. - c.89A>G r.(?) p.(His30Arg)
-?/. - c.90C>T r.(?) p.(His30=)
-?/. - c.135_137del r.(?) p.(Ser60del)
-?/. - c.135_137del r.(?) p.(Ser60del)
?/. - c.135_137del r.(?) p.(Ser60del)
-/. - c.135_137dup r.(?) p.(Ser60dup)
-/. - c.135_137dup r.(?) p.(Ser60dup)
?/. - c.141_149del r.(?) p.(Ser58_Ser60del)
?/. - c.176C>T r.(?) p.(Ser59Phe)
?/. - c.187G>T r.(?) p.(Glu63Ter)
-?/. - c.365G>C r.(?) p.(Gly122Ala)
?/. - c.378+256T>C r.(=) p.(=)
?/. - c.378+266G>A r.(=) p.(=)
?/. - c.378+323G>A r.(=) p.(=)
-?/. - c.378+372G>C r.(=) p.(=)
-?/. - c.378+621del r.(=) p.(=)
-?/. - c.378+757A>G r.(=) p.(=)
-?/. - c.378+771G>C r.(=) p.(=)
-?/. - c.378+830C>T r.(=) p.(=)
-?/. - c.378+851C>T r.(=) p.(=)
-?/. - c.378+867C>T r.(=) p.(=)
-?/. - c.378+868G>A r.(=) p.(=)
-/. - c.378+897C>G r.(=) p.(=)
-?/. - c.378+1008A>G r.(=) p.(=)
-?/. - c.378+6292C>T r.(=) p.(=)
-?/. 1i c.379-9290G>A r.(?) p.(=)
-?/. - c.413C>T r.(?) p.(Ala138Val)
-?/. - c.414G>A r.(?) p.(Ala138=)
?/. - c.460G>T r.(?) p.(Ala154Ser)
?/. - c.514G>A r.(?) p.(Ala172Thr)
-?/. - c.540+135C>T r.(=) p.(=)
-?/. - c.603-32648C>T r.(=) p.(=)
-?/. - c.603-123del r.(=) p.(=)
-?/. - c.603-89C>T r.(=) p.(=)
-?/. - c.651C>T r.(?) p.(Ile217=)
-/. - c.687C>T r.(?) p.(Phe229=)
-/. - c.696+13A>G r.(=) p.(=)
-/. - c.697-100A>G r.(=) p.(=)
-?/. - c.762G>A r.(?) p.(Thr254=)
+/. - c.826G>C r.(?) p.(Ala276Pro)
-/. - c.884+169C>T r.(=) p.(=)
-/. - c.885-81G>A r.(=) p.(=)
-?/. - c.945C>T r.(?) p.(Ala315=)
-/. - c.960+48C>A r.(=) p.(=)
?/. - c.1066G>C r.(?) p.(Gly356Arg)
+?/. 8 c.1127G>T r.(?) p.(Gly376Val)
+?/. - c.1148A>C r.(?) p.(Tyr383Ser)
-/. - c.1223+71_1223+73del r.(=) p.(=)
-/. - c.1224-52G>C r.(=) p.(=)
-?/. - c.1224-8C>T r.(=) p.(=)
?/. - c.1238G>A r.(?) p.(Cys413Tyr)
-?/. - c.1239C>T r.(?) p.(Cys413=)
-?/. - c.1239C>T r.(?) p.(Cys413=)
-?/. - c.1288C>A r.(?) p.(His430Asn)
-?/. - c.1320C>T r.(?) p.(Ile440=)
-?/. - c.1320C>T r.(?) p.(Ile440=)
?/. - c.1358A>T r.(?) p.(Glu453Val)
-?/. - c.1455T>C r.(?) p.(Asp485=)
-?/. - c.1524-63A>G r.(=) p.(=)
-?/. 13 c.1554G>T r.(?) p.(Lys518Asn)
?/. - c.1554G>T r.(?) p.(Lys518Asn)
-?/. - c.1563C>A r.(?) p.(Ile521=)
-?/. - c.1563C>A r.(?) p.(Ile521=)
-?/. - c.1593+43C>T r.(=) p.(=)
-?/. - c.1593+426C>T r.(=) p.(=)
?/. - c.1606A>C r.(?) p.(Asn536His)
-?/. - c.1632A>C r.(?) p.(Glu544Asp)
-?/. - c.1749+6G>A r.(=) p.(=)
-?/. - c.1749+11G>A r.(=) p.(=)
+/. - c.1766G>A r.(?) p.(Trp589*)
-?/. - c.1842C>T r.(?) p.(Ser614=)
-?/. - c.1917C>T r.(?) p.(Asn639=)
-/. - c.1929-241G>T r.(=) p.(=)
-/. - c.1929-162T>C r.(=) p.(=)
-?/. - c.1934G>A r.(?) p.(Arg645Gln)
-?/. - c.1940+14G>A r.(=) p.(=)
-?/. - c.1940+165A>G r.(=) p.(=)
-/. - c.1940+2410G>A r.(=) p.(=)
-?/. - c.1941-173A>G r.(=) p.(=)
-?/. 18 c.1979A>C r.(?) p.(Glu660Ala)
-?/. - c.2027+7G>A r.(=) p.(=)
-?/. - c.2028-699T>A r.(=) p.(=)
-?/. - c.2028-572G>C r.(=) p.(=)
?/. - c.2056G>A r.(?) p.(Asp686Asn)
?/. - c.2102G>A r.(?) p.(Arg701Gln)
-?/. - c.2104+3600C>T r.(=) p.(=)
-?/. - c.2104+3753A>G r.(=) p.(=)
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