Colon Cancer: Gene >> TBXA2R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375190
Start	3595735:3595735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985T>C
AA Mutation	p.Ser329Pro(p.S329P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375190
Start	3599962:3599962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746714945
CDS Mutation	c.673G>A
AA Mutation	p.Val225Ile(p.V225I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375190
Start	3600219:3600219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>T
AA Mutation	p.Ser139Leu(p.S139L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375190
Start	3600321:3600321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>A
AA Mutation	p.Cys105Tyr(p.C105Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375190
Start	3600190:3600190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>A
AA Mutation	p.Ala149Thr(p.A149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3599999:3599999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3600560:3600560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3600494:3600494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3599870:3599870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775983717
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3600545:3600545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3600431:3600431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3595784:3595784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375190
Start	3600125:3600125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TBXA2R

No Mutation Annotation!