Colon Cancer: Gene >> FUT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314412
Start	137031171:137031171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568T>C
AA Mutation	p.Tyr190His(p.Y190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314412
Start	137031531:137031531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117125309
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Cys(p.R70C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314412
Start	137030799:137030799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751960711
CDS Mutation	c.940C>T
AA Mutation	p.Arg314Trp(p.R314W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314412
Start	137031692:137031692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>T
AA Mutation	p.Gly16Val(p.G16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314412
Start	137031071:137031071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748230192
CDS Mutation	c.668G>A
AA Mutation	p.Arg223His(p.R223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314412
Start	137031629:137031629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110C>T
AA Mutation	p.Pro37Leu(p.P37L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314412
Start	137030860:137030860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314412
Start	137031617:137031617(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.122delC
AA Mutation	p.Pro41ArgfsTer38(p.P41Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FUT7

No Mutation Annotation!