Colon Cancer: Gene >> ST3GAL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377332
Start	85848134:85848134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140019292
CDS Mutation	c.389C>T
AA Mutation	p.Ala130Val(p.A130V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377332
Start	85840154:85840154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200683924
CDS Mutation	c.1247G>A
AA Mutation	p.Arg416His(p.R416H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377332
Start	85844487:85844487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917T>C
AA Mutation	p.Phe306Ser(p.F306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ST3GAL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377332
Start	85840218:85840218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183A>G
AA Mutation	p.Thr395Ala(p.T395A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377332
Start	85848145:85848145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>T
AA Mutation	p.Lys126Asn(p.K126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377332
Start	85844507:85844507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript