Colon Cancer: Gene >> TSPAN6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373020
Start	100636636:100636636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59T>C
AA Mutation	p.Val20Ala(p.V20A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373020
Start	100635745:100635745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89T>C
AA Mutation	p.Ile30Thr(p.I30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373020
Start	100633995:100633995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>A
AA Mutation	p.Ala129Asp(p.A129D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373020
Start	100636689:100636689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373020
Start	100636623:100636623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373020
Start	100635693:100635693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373020
Start	100635202:100635202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TSPAN6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373020
Start	100632536:100632536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618G>T
AA Mutation	p.Glu206Asp(p.E206D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript