Colon Cancer: Gene >> TCEA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53970448:53970448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Ala281Thr(p.A281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53979063:53979063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787T>C
AA Mutation	p.Cys263Arg(p.C263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53988186:53988186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199869556
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Trp(p.R132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53979108:53979108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762271675
CDS Mutation	c.742C>T
AA Mutation	p.His248Tyr(p.H248Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53979141:53979141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Trp(p.R237W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53993726:53993726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Glu88Lys(p.E88K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TCEA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53988122:53988122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764364857
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000521604
Start	53993726:53993726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Glu88Lys(p.E88K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript