Mutation

Primary Site >> Pancreatic Cancer

Gene >> MYH14

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50309170:50309170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369147236
CDS Mutation	c.5830C>T
AA Mutation	p.Arg1944Trp(p.R1944W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50276032:50276032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3386C>A
AA Mutation	p.Ser1129Tyr(p.S1129Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50301724:50301724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199600574
CDS Mutation	c.5410C>T
AA Mutation	p.Arg1804Trp(p.R1804W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50223339:50223339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683C>A
AA Mutation	p.Pro228Gln(p.P228Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50289547:50289547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4741C>T
AA Mutation	p.Arg1581Cys(p.R1581C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50301695:50301695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754861302
CDS Mutation	c.5381G>A
AA Mutation	p.Arg1794His(p.R1794H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50293663:50293663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5322C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50250519:50250520(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1643dupC
AA Mutation	p.Gly549TrpfsTer8(p.G549Wfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript