Colon Cancer: Gene >> CRHR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30662723:30662723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668G>A
AA Mutation	p.Arg223His(p.R223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30655651:30655651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764886717
CDS Mutation	c.982G>A
AA Mutation	p.Val328Ile(p.V328I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30662746:30662746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645G>T
AA Mutation	p.Met215Ile(p.M215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30662730:30662730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767864800
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30665609:30665609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200310748
CDS Mutation	c.346G>A
AA Mutation	p.Ala116Thr(p.A116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000471646
Start	30665531:30665531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Trp(p.R142W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471646
Start	30655983:30655983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471646
Start	30655072:30655072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552742156
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471646
Start	30682206:30682206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CRHR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348438
Start	30699997:30699997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548065920
CDS Mutation	c.37G>A
AA Mutation	p.Val13Ile(p.V13I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30665159:30665159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454C>T
AA Mutation	p.His152Tyr(p.H152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30653500:30653500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143322026
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399Gln(p.R399Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000471646
Start	30665128:30665128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776086218
CDS Mutation	c.485G>A
AA Mutation	p.Arg162Gln(p.R162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471646
Start	30653586:30653586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471646
Start	30655072:30655072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552742156
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript