Colon Cancer: Gene >> C4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435363
Start	32029312:32029312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3650T>C
AA Mutation	p.Leu1217Pro(p.L1217P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000435363
Start	32027109:32027109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2579A>G
AA Mutation	p.Asp860Gly(p.D860G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000435363
Start	32029188:32029188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3526A>C
AA Mutation	p.Ser1176Arg(p.S1176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000435363
Start	32027312:32027312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2669C>A
AA Mutation	p.Pro890His(p.P890H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435363
Start	32027337:32027337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2694C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435363
Start	32029175:32029175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3513C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> C4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435363
Start	32029205:32029205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3543G>T
AA Mutation	p.Glu1181Asp(p.E1181D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435363
Start	32029690:32029690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373001823
CDS Mutation	c.3801C>T
Mutation Classification	Silent
Feature Type	Transcript