Colon Cancer: Gene >> GPR143

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000467482
Start	9743610:9743610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722T>C
AA Mutation	p.Val241Ala(p.V241A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000467482
Start	9739545:9739545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060G>A
AA Mutation	p.Gly354Arg(p.G354R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000467482
Start	9739637:9739637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968C>A
AA Mutation	p.Pro323His(p.P323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467482
Start	9760768:9760768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770611660
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467482
Start	9746087:9746087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000467482
Start	9759388:9759388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399G>A
AA Mutation	p.Trp133Ter(p.W133*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPR143

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000467482
Start	9741447:9741447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>T
AA Mutation	p.Ser259Leu(p.S259L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467482
Start	9743615:9743615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717A>G
Mutation Classification	Silent
Feature Type	Transcript