Colon Cancer: Gene >> MSR1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262101
Start	16155064:16155064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898G>T
AA Mutation	p.Gly300Cys(p.G300C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16175200:16175200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204T>G
AA Mutation	p.Ile68Met(p.I68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262101
Start	16164067:16164067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815A>C
AA Mutation	p.Gln272Pro(p.Q272P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16164072:16164072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810A>T
AA Mutation	p.Leu270Phe(p.L270F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16155115:16155115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847G>T
AA Mutation	p.Asp283Tyr(p.D283Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16168775:16168775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs13306549
CDS Mutation	c.313G>A
AA Mutation	p.Glu105Lys(p.E105K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16177977:16177977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12G>T
AA Mutation	p.Trp4Cys(p.W4C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16120445:16120445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>A
AA Mutation	p.Val399Met(p.V399M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16120477:16120477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163G>A
AA Mutation	p.Cys388Tyr(p.C388Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262101
Start	16168749:16168749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262101
Start	16120563:16120563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262101
Start	16168584:16168584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000262101
Start	16168754:16168754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>T
AA Mutation	p.Glu112Ter(p.E112*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000262101
Start	16164186:16164187(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.695_696insTATATATCATTTTCTGGAGAAATG
AA Mutation	p.Glu232delinsAspIleTyrHisPheLeuGluLysTer(p.E232delinsDIYHFLEK*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16120511:16120511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>A
AA Mutation	p.Asp377Asn(p.D377N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16150234:16150234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976C>T
AA Mutation	p.Pro326Ser(p.P326S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262101
Start	16175301:16175301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript