Colon Cancer: Gene >> TOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58807769:58807769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559A>G
AA Mutation	p.Asp520Gly(p.D520G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58815669:58815669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200969018
CDS Mutation	c.1061C>T
AA Mutation	p.Ser354Leu(p.S354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58851802:58851802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415C>T
AA Mutation	p.Pro139Ser(p.P139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58838266:58838266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201277886
CDS Mutation	c.739C>A
AA Mutation	p.Pro247Thr(p.P247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58815568:58815568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162A>G
AA Mutation	p.Met388Val(p.M388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58838272:58838272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733A>G
AA Mutation	p.Lys245Glu(p.K245E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58815697:58815697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033A>C
AA Mutation	p.Thr345Pro(p.T345P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	59118980:59118980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8T>C
AA Mutation	p.Val3Ala(p.V3A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58808132:58808132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>G
AA Mutation	p.Asp510Glu(p.D510E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58826891:58826891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936G>T
AA Mutation	p.Lys312Asn(p.K312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361421
Start	58826897:58826897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370108565
CDS Mutation	c.930T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000361421
Start	58851793:58851793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Ter(p.R142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000361421
Start	58815471:58815473(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1257_1259delTCC
AA Mutation	p.Pro420del(p.P420del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58826891:58826891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936G>T
AA Mutation	p.Lys312Asn(p.K312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58838181:58838181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824C>A
AA Mutation	p.Thr275Asn(p.T275N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361421
Start	58815669:58815669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200969018
CDS Mutation	c.1061C>T
AA Mutation	p.Ser354Leu(p.S354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361421
Start	58939383:58939383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330A>C
Mutation Classification	Silent
Feature Type	Transcript