Colon Cancer: Gene >> C2orf40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238044
Start	106073982:106073982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368622171
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238044
Start	106077906:106077906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376920426
CDS Mutation	c.427G>A
AA Mutation	p.Val143Ile(p.V143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238044
Start	106077827:106077827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150617664
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000238044
Start	106077910:106077911(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.431_432insATTT
AA Mutation	p.Asn144LysfsTer5(p.N144Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> C2orf40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238044
Start	106071881:106071881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117A>C
AA Mutation	p.Gln39His(p.Q39H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238044
Start	106077855:106077855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376G>T
AA Mutation	p.Asp126Tyr(p.D126Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238044
Start	106077807:106077807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328A>C
AA Mutation	p.Asn110His(p.N110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript