Colon Cancer: Gene >> GPR34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41696667:41696667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345Gln(p.R345Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41696580:41696580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947C>T
AA Mutation	p.Ser316Leu(p.S316L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41696394:41696394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>C
AA Mutation	p.Lys254Thr(p.K254T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41696577:41696577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944T>G
AA Mutation	p.Leu315Arg(p.L315R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41696643:41696643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010T>C
AA Mutation	p.Ile337Thr(p.I337T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41695884:41695884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378138
Start	41696574:41696574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941T>C
AA Mutation	p.Val314Ala(p.V314A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378138
Start	41695645:41695645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378138
Start	41695855:41695855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000378138
Start	41695835:41695835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>T
AA Mutation	p.Gly68Ter(p.G68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPR34

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000378138
Start	41695961:41695961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Ter(p.R110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript