Colon Cancer: Gene >> CD44

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428726
Start	35176599:35176599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92C>T
AA Mutation	p.Ala31Val(p.A31V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428726
Start	35196866:35196866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567538684
CDS Mutation	c.788A>G
AA Mutation	p.Gln263Arg(p.Q263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428726
Start	35186836:35186836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000428726
Start	35198120:35198120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CD44

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428726
Start	35198205:35198205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>A
AA Mutation	p.Gly294Glu(p.G294E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428726
Start	35201686:35201686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052G>A
AA Mutation	p.Gly351Asp(p.G351D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript