Colon Cancer: Gene >> SLC38A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256689
Start	46362521:46362521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773343163
CDS Mutation	c.1297A>G
AA Mutation	p.Thr433Ala(p.T433A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256689
Start	46361180:46361180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256689
Start	46363785:46363786(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.994_995insGTTTTTGTTTTTG
AA Mutation	p.Phe332CysfsTer28(p.F332Cfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256689
Start	46371279:46371280(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.14_15insTAGCAAATTAAAGC
AA Mutation	p.Glu5AspfsTer38(p.E5Dfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC38A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256689
Start	46364499:46364499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139420539
CDS Mutation	c.763G>A
AA Mutation	p.Glu255Lys(p.E255K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256689
Start	46367336:46367336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>A
AA Mutation	p.Leu107Ile(p.L107I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256689
Start	46367164:46367164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393T>A
Mutation Classification	Silent
Feature Type	Transcript