Mutation

Primary Site >> Stomach Cancer

Gene >> FEN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61795936:61795936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778764875
CDS Mutation	c.575G>A
AA Mutation	p.Arg192Gln(p.R192Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61795836:61795836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778852873
CDS Mutation	c.475G>A
AA Mutation	p.Ala159Thr(p.A159T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796425:61796425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761723999
CDS Mutation	c.1064G>A
AA Mutation	p.Arg355His(p.R355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796320:61796320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959G>A
AA Mutation	p.Arg320Gln(p.R320Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796326:61796326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756180049
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61795669:61795669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762018999
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305885
Start	61795466:61795466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305885
Start	61795959:61795959(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.602delA
AA Mutation	p.Lys201SerfsTer9(p.K201Sfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript