Colon Cancer: Gene >> SLC38A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000595796
Start	48459761:48459761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184C>A
AA Mutation	p.Pro395Gln(p.P395Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595796
Start	48460688:48460688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595796
Start	48467015:48467015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782267859
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595796
Start	48466842:48466842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782434538
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000595796
Start	48461768:48461768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.801delT
AA Mutation	p.Phe267LeufsTer54(p.F267Lfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC38A5

No Mutation Annotation!