Colon Cancer: Gene >> USP14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261601
Start	198113:198113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Gly248Ser(p.G248S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261601
Start	163331:163331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40A>C
AA Mutation	p.Lys14Gln(p.K14Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261601
Start	179025:179025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288G>T
AA Mutation	p.Gln96His(p.Q96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261601
Start	196734:196734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374980775
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000261601
Start	179023:179024(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.287_288insCATATAACATAATTCTA
AA Mutation	p.Gln96HisfsTer3(p.Q96Hfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261601
Start	203145:203146(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.997dupT
AA Mutation	p.Tyr333LeufsTer2(p.Y333Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000261601
Start	199221:199223(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758112641
CDS Mutation	c.791_793delAAG
AA Mutation	p.Glu264del(p.E264del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> USP14

No Mutation Annotation!