Colon Cancer: Gene >> TAS2R14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000537503
Start	10938621:10938621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587C>T
AA Mutation	p.Ala196Val(p.A196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000537503
Start	10938330:10938330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878C>T
AA Mutation	p.Ser293Leu(p.S293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537503
Start	10939031:10939031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000537503
Start	10938825:10938825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.383delA
AA Mutation	p.Lys128ArgfsTer9(p.K128Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TAS2R14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000537503
Start	10938795:10938795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758340538
CDS Mutation	c.413C>T
AA Mutation	p.Ser138Leu(p.S138L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000537503
Start	10938898:10938898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310G>A
AA Mutation	p.Gly104Ser(p.G104S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000537503
Start	10938550:10938550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773473266
CDS Mutation	c.658G>A
AA Mutation	p.Gly220Arg(p.G220R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript