Colon Cancer: Gene >> ING5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313552
Start	241725004:241725004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696T>G
AA Mutation	p.Cys232Trp(p.C232W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313552
Start	241709243:241709243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137C>T
AA Mutation	p.Ala46Val(p.A46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313552
Start	241709261:241709261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375367616
CDS Mutation	c.155C>T
AA Mutation	p.Thr52Met(p.T52M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313552
Start	241723009:241723009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Glu185Lys(p.E185K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313552
Start	241709316:241709316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200433676
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313552
Start	241723008:241723008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537761072
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313552
Start	241712011:241712011(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.425delG
AA Mutation	p.Gly142AlafsTer58(p.G142Afs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000313552
Start	241712016:241712016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758519998
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Ter(p.R143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000313552
Start	241709340:241709340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234C>A
AA Mutation	p.Tyr78Ter(p.Y78*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ING5

No Mutation Annotation!