Colon Cancer: Gene >> TCN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215838
Start	30623053:30623053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192C>A
AA Mutation	p.Leu398Ile(p.L398I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215838
Start	30623024:30623024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774428161
CDS Mutation	c.1163C>T
AA Mutation	p.Ala388Val(p.A388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215838
Start	30615724:30615724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>G
AA Mutation	p.Leu293Val(p.L293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215838
Start	30610928:30610928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>T
AA Mutation	p.Trp41Leu(p.W41L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000215838
Start	30617387:30617387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117458738
CDS Mutation	c.998C>T
AA Mutation	p.Thr333Met(p.T333M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215838
Start	30612981:30612981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215838
Start	30617442:30617442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142555281
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215838
Start	30615614:30615614(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.771delC
AA Mutation	p.Met258CysfsTer31(p.M258Cfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000215838
Start	30610929:30610929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>A
AA Mutation	p.Trp41Ter(p.W41*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215838
Start	30607372:30607373(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.46dupG
AA Mutation	p.Ala16GlyfsTer4(p.A16Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215838
Start	30610884:30610884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>T
AA Mutation	p.Met26Ile(p.M26I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript