Colon Cancer: Gene >> GPR65

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267549
Start	88011149:88011149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302G>A
AA Mutation	p.Ser101Asn(p.S101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267549
Start	88011521:88011521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674T>A
AA Mutation	p.Ile225Lys(p.I225K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267549
Start	88011552:88011552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267549
Start	88010859:88010859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267549
Start	88011711:88011711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267549
Start	88011621:88011621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781265796
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR65

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267549
Start	88011328:88011328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>A
AA Mutation	p.Asp161Asn(p.D161N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript