Colon Cancer: Gene >> GRPR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380289
Start	16150349:16150349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458C>T
AA Mutation	p.Ala153Val(p.A153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380289
Start	16150549:16150549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143721353
CDS Mutation	c.658G>A
AA Mutation	p.Val220Ile(p.V220I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380289
Start	16152592:16152592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>A
AA Mutation	p.Val368Met(p.V368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380289
Start	16150466:16150466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575C>A
AA Mutation	p.Thr192Asn(p.T192N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380289
Start	16150553:16150553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662T>A
AA Mutation	p.Ile221Asn(p.I221N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380289
Start	16150467:16150467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380289
Start	16150359:16150359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380289
Start	16124037:16124037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380289
Start	16124232:16124232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GRPR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380289
Start	16150523:16150523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>A
AA Mutation	p.Ser211Tyr(p.S211Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript