Colon Cancer: Gene >> ADAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602002:154602002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>A
AA Mutation	p.Asp214Asn(p.D214N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154590380:154590380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2300G>T
AA Mutation	p.Arg767Leu(p.R767L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602509:154602509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133G>C
AA Mutation	p.Glu45Gln(p.E45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154584830:154584830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3657G>T
AA Mutation	p.Lys1219Asn(p.K1219N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154601308:154601308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1334G>T
AA Mutation	p.Gly445Val(p.G445V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602357:154602357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285G>T
AA Mutation	p.Arg95Ser(p.R95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154589790:154589790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2635G>A
AA Mutation	p.Glu879Lys(p.E879K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154585268:154585268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3392C>T
AA Mutation	p.Ala1131Val(p.A1131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154584910:154584910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3577G>A
AA Mutation	p.Glu1193Lys(p.E1193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602620:154602620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22T>A
AA Mutation	p.Ser8Thr(p.S8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602287:154602287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>T
AA Mutation	p.Pro119Ser(p.P119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602325:154602325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>A
AA Mutation	p.Arg106Lys(p.R106K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602373:154602373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269T>G
AA Mutation	p.Ile90Ser(p.I90S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154588632:154588632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767879893
CDS Mutation	c.2804C>T
AA Mutation	p.Ala935Val(p.A935V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154601750:154601750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755166511
CDS Mutation	c.892G>A
AA Mutation	p.Glu298Lys(p.E298K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154588162:154588162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2982T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154601967:154601967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771459105
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154601100:154601100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757137562
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000368474
Start	154602383:154602383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259C>T
AA Mutation	p.Gln87Ter(p.Q87*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154585862:154585862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3206A>C
AA Mutation	p.Tyr1069Ser(p.Y1069S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154589456:154589456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs398122892
CDS Mutation	c.2675G>A
AA Mutation	p.Arg892His(p.R892H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154601079:154601079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1563C>A
AA Mutation	p.Phe521Leu(p.F521L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154601900:154601900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742G>A
AA Mutation	p.Val248Ile(p.V248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154588168:154588168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552926126
CDS Mutation	c.2976C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154602237:154602237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000368474
Start	154597948:154597948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1814C>G
AA Mutation	p.Ser605Ter(p.S605*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript