Colon Cancer: Gene >> TCEAL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372774
Start	102141189:102141189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372774
Start	102140971:102140971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361T>C
AA Mutation	p.Ser121Pro(p.S121P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372774
Start	102141041:102141041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372774
Start	102141323:102141323(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.9delA
AA Mutation	p.Lys3AsnfsTer20(p.K3Nfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000372774
Start	102141205:102141205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>T
AA Mutation	p.Glu43Ter(p.E43*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372774
Start	102140980:102140981(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.351dupG
AA Mutation	p.Thr118AspfsTer20(p.T118Dfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCEAL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372774
Start	102140979:102140979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353C>T
AA Mutation	p.Thr118Met(p.T118M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript