Colon Cancer: Gene >> MARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57500424:57500424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777616090
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Cys(p.R399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57498227:57498227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841C>A
AA Mutation	p.Leu281Ile(p.L281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57500503:57500503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274T>C
AA Mutation	p.Ile425Thr(p.I425T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57490279:57490279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>T
AA Mutation	p.Thr188Ile(p.T188I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57498216:57498216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>G
AA Mutation	p.Asn277Ser(p.N277S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57514962:57514962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2108A>G
AA Mutation	p.Asp703Gly(p.D703G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57498536:57498536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004A>C
AA Mutation	p.Lys335Thr(p.K335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57512263:57512263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663G>T
AA Mutation	p.Asp555Tyr(p.D555Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57490598:57490598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724A>C
AA Mutation	p.Lys242Gln(p.K242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57500392:57500392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163G>A
AA Mutation	p.Arg388Gln(p.R388Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262027
Start	57490558:57490558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262027
Start	57514795:57514795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2043G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262027
Start	57512827:57512827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149742633
CDS Mutation	c.1830G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262027
Start	57489333:57489333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752312333
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000262027
Start	57516247:57516247(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2470delA
AA Mutation	p.Thr824ArgfsTer8(p.T824Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57516468:57516468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2590G>T
AA Mutation	p.Ala864Ser(p.A864S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57515043:57515043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2189G>A
AA Mutation	p.Gly730Asp(p.G730D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57490305:57490305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589G>A
AA Mutation	p.Ala197Thr(p.A197T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262027
Start	57511789:57511789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1460G>A
AA Mutation	p.Arg487Gln(p.R487Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000262027
Start	57516450:57516450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2572G>T
AA Mutation	p.Glu858Ter(p.E858*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript