Colon Cancer: Gene >> TSPAN7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378482
Start	38666283:38666283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244C>T
AA Mutation	p.Arg82Cys(p.R82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378482
Start	38561617:38561617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71T>C
AA Mutation	p.Phe24Ser(p.F24S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378482
Start	38681223:38681223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617C>T
AA Mutation	p.Thr206Ile(p.T206I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378482
Start	38675775:38675775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512C>T
AA Mutation	p.Pro171Leu(p.P171L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378482
Start	38681266:38681266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763482838
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378482
Start	38675794:38675794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761317239
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378482
Start	38687622:38687622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378482
Start	38675773:38675773(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752121179
CDS Mutation	c.516delC
AA Mutation	p.Ser173AlafsTer4(p.S173Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TSPAN7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378482
Start	38681214:38681214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608A>C
AA Mutation	p.Asp203Ala(p.D203A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript