Colon Cancer: Gene >> TFEB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230323
Start	41691176:41691176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775220771
CDS Mutation	c.38G>A
AA Mutation	p.Arg13Gln(p.R13Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230323
Start	41689775:41689775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505G>A
AA Mutation	p.Asp169Asn(p.D169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230323
Start	41690839:41690839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292G>A
AA Mutation	p.Glu98Lys(p.E98K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230323
Start	41691192:41691192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22C>T
AA Mutation	p.Arg8Cys(p.R8C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230323
Start	41690744:41690744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756151147
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230323
Start	41684953:41684953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1077C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230323
Start	41689782:41689782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TFEB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230323
Start	41684727:41684727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303C>G
AA Mutation	p.Leu435Val(p.L435V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230323
Start	41690729:41690729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777139304
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230323
Start	41690786:41690786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555070268
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript