Colon Cancer: Gene >> TAS1R3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1332426:1332426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895G>T
AA Mutation	p.Ala299Ser(p.A299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1332670:1332670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139A>T
AA Mutation	p.Asn380Ile(p.N380I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1332640:1332640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109G>A
AA Mutation	p.Cys370Tyr(p.C370Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1333875:1333875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1970A>G
AA Mutation	p.Glu657Gly(p.E657G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1333677:1333677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772T>C
AA Mutation	p.Val591Ala(p.V591A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1332574:1332574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043C>A
AA Mutation	p.Pro348Gln(p.P348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1334294:1334294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2389G>A
AA Mutation	p.Ala797Thr(p.A797T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1334079:1334079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748069550
CDS Mutation	c.2174G>A
AA Mutation	p.Arg725His(p.R725H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1333691:1333691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1786A>C
AA Mutation	p.Ser596Arg(p.S596R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339381
Start	1333519:1333519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1614C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339381
Start	1331456:1331456(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs765718073
CDS Mutation	c.117delG
AA Mutation	p.Leu40CysfsTer37(p.L40Cfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339381
Start	1333711:1333711(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777573279
CDS Mutation	c.1812delG
AA Mutation	p.Leu606TrpfsTer43(p.L606Wfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000339381
Start	1333029:1333029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384C>T
AA Mutation	p.Gln462Ter(p.Q462*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000339381
Start	1333597:1333597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762273197
CDS Mutation	c.1692G>A
AA Mutation	p.Trp564Ter(p.W564*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339381
Start	1332688:1332689(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1158dupT
AA Mutation	p.His387SerfsTer13(p.H387Sfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TAS1R3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339381
Start	1331438:1331438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93G>T
AA Mutation	p.Met31Ile(p.M31I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript