Transcript #00025634 (NM_006258.3, PRKG1 gene)

Transcript name transcript variant 2
Gene name PRKG1 (protein kinase, cGMP-dependent, type I)
Chromosome 10
Transcript - NCBI ID NM_006258.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006249.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2021-08-23 16:49:09 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. _1 c.-83181T>C r.(?) p.(=)
?/. _1 c.-83174G>A r.(?) p.(=)
-?/. _1 c.-83174G>A r.(?) p.(=)
-?/. - c.-83126G>A r.(?) p.(=)
?/. _1 c.-83079C>A r.(?) p.(=)
-?/. - c.-82916C>G r.(?) p.(=)
-?/. - c.30G>A r.(?) p.(=)
-?/. - c.197G>T r.(?) p.(Ser66Ile)
?/. - c.322C>T r.(?) p.(Leu108Phe)
-?/. - c.395A>G r.(?) p.(Asp132Gly)
?/. - c.401T>C r.(?) p.(Met134Thr)
?/. - c.404A>C r.(?) p.(Asp135Ala)
-/. - c.408G>A r.(?) p.(Pro136=)
?/. - c.421A>G r.(?) p.(Lys141Glu)
?/. - c.421A>G r.(?) p.(Lys141Glu)
-/. - c.426C>T r.(?) p.(Asp142=)
-/. - c.426C>T r.(?) p.(Asp142=)
-?/. - c.426C>T r.(?) p.(Asp142=)
+?/. - c.(433+1_434-1)_(547+1_548-1)del r.(434_547del) p.(Asp145_Thr183delinsAla)
?/. - c.449A>C r.(?) p.(Asp150Ala)
?/. - c.449A>C r.(?) p.(Asp150Ala)
?/. - c.454G>C r.(?) p.(Gly152Arg)
-/. - c.479-9C>T r.(=) p.(=)
+?/. - c.(478+1_479-1)_(592+1_593-1)del r.? p.(Asp160_Thr198delinsAla)
?/. - c.520A>T r.(?) p.(Thr174Ser)
-?/. - c.522C>T r.(?) p.(Thr174=)
+/. - c.530G>A r.(?) p.(Arg177Gln)
+/. - c.575G>A r.(?) p.(Arg192Gln)
+/. - c.575G>A r.(?) p.(Arg192Gln)
+/. - c.575G>A r.(?) p.(Arg192Gln)
?/. - c.578C>T r.(?) p.(Thr193Ile)
?/. - c.593-106153C>T r.(=) p.(=)
-?/. - c.593-105748_593-105743del r.(=) p.(=)
-?/. - c.593-105717G>T r.(=) p.(=)
?/. - c.593-105347A>G r.(=) p.(=)
?/. - c.593-105347A>G r.(=) p.(=)
?/. - c.626G>A r.(?) p.(Arg209Gln)
-/. - c.675C>T r.(?) p.(Thr225=)
-?/. - c.675C>T r.(?) p.(Thr225=)
-?/. - c.717C>A r.(?) p.(Ser239Arg)
?/. - c.762+25494A>G r.(=) p.(=)
?/. - c.762+25494A>G r.(=) p.(=)
?/. - c.762+25580A>G r.(=) p.(=)
?/. - c.762+25580A>G r.(=) p.(=)
?/. - c.762+25639C>T r.(=) p.(=)
?/. - c.762+25639C>T r.(=) p.(=)
?/. - c.762+25745A>G r.(=) p.(=)
?/. - c.762+25745A>G r.(=) p.(=)
-?/. - c.763-71T>C r.(=) p.(=)
-/. - c.763-15G>T r.(=) p.(=)
-?/. - c.792C>T r.(?) p.(Ile264=)
-?/. - c.840+14G>T r.(=) p.(=)
-?/. - c.841-29A>T r.(=) p.(=)
-?/. - c.841-9T>C r.(=) p.(=)
-/. - c.845A>G r.(?) p.(Asn282Ser)
-/. - c.845A>G r.(?) p.(Asn282Ser)
-/. - c.845A>G r.(?) p.(Asn282Ser)
-/. - c.888T>C r.(?) p.(Leu296=)
-/. - c.888T>C r.(?) p.(Leu296=)
-?/. - c.906A>C r.(?) p.(Gly302=)
?/. - c.971T>C r.(?) p.(Leu324Ser)
-?/. - c.1002-70T>C r.(=) p.(=)
-?/. - c.1002-12T>C r.(=) p.(=)
-?/. - c.1002-9G>A r.(=) p.(=)
-?/. - c.1002-9G>A r.(=) p.(=)
-?/. - c.1002-9G>A r.(=) p.(=)
-/. - c.1008T>C r.(?) p.(Phe336=)
?/. - c.1016T>C r.(?) p.(Leu339Ser)
?/. - c.1016T>C r.(?) p.(Leu339Ser)
?/. - c.1016T>C r.(?) p.(Leu339Ser)
?/. - c.1016T>C r.(?) p.(Leu339Ser)
-?/. - c.1026G>A r.(?) p.(Gly342=)
-?/. - c.1026G>A r.(?) p.(Gly342=)
-?/. - c.1071A>G r.(?) p.(Lys357=)
-?/. - c.1071A>G r.(?) p.(Lys357=)
-?/. - c.1071A>G r.(?) p.(Lys357=)
-/. - c.1076+19_1076+20insTGGCCTT r.(=) p.(=)
-/. - c.1080T>C r.(?) p.(Tyr360=)
-/. - c.1080T>C r.(?) p.(Tyr360=)
?/. - c.1084G>A r.(?) p.(Ala362Thr)
-?/. - c.1092G>A r.(?) p.(Ala364=)
?/. - c.1102G>A r.(?) p.(Ala368Thr)
?/. - c.1105A>C r.(?) p.(Asn369His)
?/. - c.1106A>G r.(?) p.(Asn369Ser)
?/. - c.1166T>C r.(?) p.(Val389Ala)
?/. - c.1166T>C r.(?) p.(Val389Ala)
-?/. - c.1173+4G>A r.spl? p.?
-?/. - c.1174-9T>G r.(=) p.(=)
?/. - c.1190A>G r.(?) p.(Glu397Gly)
-?/. - c.1290G>A r.(?) p.(Gly430=)
-?/. - c.1299C>T r.(?) p.(Ser433=)
-?/. - c.1313+5del r.spl? p.?
-?/. - c.1313+10C>G r.(=) p.(=)
-?/. - c.1313+55A>G r.(=) p.(=)
-?/. - c.1314-69C>T r.(=) p.(=)
-?/. - c.1314-9A>G r.(=) p.(=)
?/. - c.1338C>A r.(?) p.(Ser446Arg)
-?/. - c.1338C>A r.(?) p.(Ser446Arg)
-?/. - c.1403+183C>A r.(=) p.(=)
-?/. - c.1403+328A>C r.(=) p.(=)
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