Colon Cancer: Gene >> ADORA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165474:203165474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>A
AA Mutation	p.Phe185Leu(p.F185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165719:203165719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800G>T
AA Mutation	p.Ser267Ile(p.S267I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203128899:203128899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>A
AA Mutation	p.Ala20Thr(p.A20T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203128845:203128845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4C>T
AA Mutation	p.Pro2Ser(p.P2S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165754:203165754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748346254
CDS Mutation	c.835G>A
AA Mutation	p.Gly279Ser(p.G279S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165429:203165429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>C
AA Mutation	p.Glu170Asp(p.E170D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165483:203165483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564G>T
AA Mutation	p.Trp188Cys(p.W188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165284:203165284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750446791
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165580:203165580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778641521
CDS Mutation	c.661G>A
AA Mutation	p.Asp221Asn(p.D221N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203165842:203165842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141819948
CDS Mutation	c.923G>A
AA Mutation	p.Arg308His(p.R308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309502
Start	203128997:203128997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309502
Start	203165294:203165294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562367584
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309502
Start	203165585:203165585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201849915
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309502
Start	203165291:203165291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143331026
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309502
Start	203165735:203165735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309502
Start	203128856:203128856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADORA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203129103:203129103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>T
AA Mutation	p.Leu88Phe(p.L88F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309502
Start	203128914:203128914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>T
AA Mutation	p.Pro25Ser(p.P25S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript