Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TAS2R38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973518:141973518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172C>A
AA Mutation	p.Leu58Met(p.L58M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973667:141973667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375588043
CDS Mutation	c.23G>A
AA Mutation	p.Arg8His(p.R8H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973559:141973559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131T>C
AA Mutation	p.Val44Ala(p.V44A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973547:141973547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143A>G
AA Mutation	p.Gln48Arg(p.Q48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973644:141973644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46A>G
AA Mutation	p.Ser16Gly(p.S16G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973128:141973128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>T
AA Mutation	p.Asp188Tyr(p.D188Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547270
Start	141973003:141973003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000547270
Start	141973200:141973201(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.489dupT
AA Mutation	p.Ser164Ter(p.S164*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TAS2R38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973245:141973245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Ile(p.L149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141972986:141972986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144212167
CDS Mutation	c.704G>A
AA Mutation	p.Arg235His(p.R235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141972791:141972791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782432120
CDS Mutation	c.899G>A
AA Mutation	p.Gly300Asp(p.G300D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000547270
Start	141973009:141973009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.681G>T
AA Mutation	p.Met227Ile(p.M227I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547270
Start	141973276:141973276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript