Colon Cancer: Gene >> TRNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251607
Start	3137448:3137448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Ala113Thr(p.A113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251607
Start	3137406:3137406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759826831
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Trp(p.R99W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251607
Start	3147950:3147950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1101G>T
AA Mutation	p.Lys367Asn(p.K367N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251607
Start	3147589:3147589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251607
Start	3140557:3140557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251607
Start	3148004:3148004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779471673
CDS Mutation	c.1155A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251607
Start	3148095:3148095(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1252delA
AA Mutation	p.Ser418ValfsTer11(p.S418Vfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251607
Start	3140638:3140639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.472_473delAT
AA Mutation	p.Met158ValfsTer5(p.M158Vfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000251607
Start	3147949:3147950(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1100_1101insAACATACAC
AA Mutation	p.Lys367_Tyr368insThrTyrThr(p.K367_Y368insTYT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251607
Start	3140621:3140621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>T
AA Mutation	p.Asp152Tyr(p.D152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251607
Start	3147508:3147508(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.865delT
AA Mutation	p.Ser289HisfsTer5(p.S289Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251607
Start	3129119:3129119(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.79delC
AA Mutation	p.Leu27TyrfsTer4(p.L27Yfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000251607
Start	3148125:3148125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>T
AA Mutation	p.Glu426Ter(p.E426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript