Colon Cancer: Gene >> HCAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328880
Start	122703145:122703145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
AA Mutation	p.Leu47Phe(p.L47F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328880
Start	122702551:122702551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733C>T
AA Mutation	p.Leu245Phe(p.L245F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328880
Start	122702887:122702887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>A
AA Mutation	p.His133Asn(p.H133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328880
Start	122702503:122702503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781T>G
AA Mutation	p.Ser261Ala(p.S261A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328880
Start	122702459:122702459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202067823
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328880
Start	122702945:122702945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328880
Start	122702495:122702495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200905506
CDS Mutation	c.789G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328880
Start	122702453:122702453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HCAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328880
Start	122702296:122702296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774860345
CDS Mutation	c.988G>A
AA Mutation	p.Glu330Lys(p.E330K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328880
Start	122702304:122702304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143584617
CDS Mutation	c.980C>T
AA Mutation	p.Thr327Met(p.T327M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328880
Start	122702198:122702198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1086T>A
Mutation Classification	Silent
Feature Type	Transcript