Colon Cancer: Gene >> TSPAN18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340160
Start	44909874:44909874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148562544
CDS Mutation	c.233G>A
AA Mutation	p.Arg78His(p.R78H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340160
Start	44909778:44909778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137C>T
AA Mutation	p.Ala46Val(p.A46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340160
Start	44909798:44909798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157A>G
AA Mutation	p.Thr53Ala(p.T53A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340160
Start	44919902:44919902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778653685
CDS Mutation	c.518C>T
AA Mutation	p.Pro173Leu(p.P173L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340160
Start	44906470:44906470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>A
AA Mutation	p.Phe18Leu(p.F18L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340160
Start	44919279:44919279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340160
Start	44919828:44919828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367945306
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340160
Start	44919903:44919903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75272704
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340160
Start	44906431:44906431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000340160
Start	44919299:44919299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>A
AA Mutation	p.Ser140Ter(p.S140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TSPAN18

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340160
Start	44926703:44926703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553812457
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000340160
Start	44919871:44919871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766678424
CDS Mutation	c.487C>T
AA Mutation	p.Arg163Ter(p.R163*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript