Colon Cancer: Gene >> ESX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104254461:104254461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Val67Ile(p.V67I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104254836:104254836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104252818:104252818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Ala173Thr(p.A173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104250278:104250278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171A>G
AA Mutation	p.Ile391Val(p.I391V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104254158:104254158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502G>C
AA Mutation	p.Ala168Pro(p.A168P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104250766:104250766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683C>T
AA Mutation	p.Ala228Val(p.A228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104254518:104254518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Trp(p.R48W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104250611:104250611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144173947
CDS Mutation	c.838T>C
AA Mutation	p.Ser280Pro(p.S280P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104250692:104250692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>T
AA Mutation	p.Pro253Ser(p.P253S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372588
Start	104254228:104254228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372588
Start	104250258:104250258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372588
Start	104250612:104250612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782474179
CDS Mutation	c.837C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372588
Start	104250330:104250330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782436242
CDS Mutation	c.1119G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372588
Start	104254186:104254186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant
Transcription ID	ENST00000372588
Start	104250896:104250898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.553-2_553delAGG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ESX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104254195:104254195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>T
AA Mutation	p.Glu155Asp(p.E155D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372588
Start	104250639:104250639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>A
AA Mutation	p.Met270Ile(p.M270I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript