Colon Cancer: Gene >> ST8SIA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268164
Start	92434356:92434356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271A>G
AA Mutation	p.Thr91Ala(p.T91A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268164
Start	92444780:92444780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.693C>A
AA Mutation	p.His231Gln(p.H231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268164
Start	92464332:92464332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>T
AA Mutation	p.His359Tyr(p.H359Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268164
Start	92444754:92444754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201692548
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Trp(p.R223W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268164
Start	92444828:92444828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142357478
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268164
Start	92444717:92444717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268164
Start	92464256:92464256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268164
Start	92394148:92394148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268164
Start	92438593:92438593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ST8SIA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268164
Start	92444772:92444772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268164
Start	92444922:92444922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772349659
CDS Mutation	c.835G>A
AA Mutation	p.Val279Ile(p.V279I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript