Colon Cancer: Gene >> ST3GAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133465967:133465967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145826176
CDS Mutation	c.430G>A
AA Mutation	p.Val144Ile(p.V144I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133476012:133476012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771438014
CDS Mutation	c.13C>T
AA Mutation	p.Arg5Trp(p.R5W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133461969:133461969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755T>G
AA Mutation	p.Ile252Ser(p.I252S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133464889:133464889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572A>G
AA Mutation	p.Tyr191Cys(p.Y191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133464833:133464833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628A>G
AA Mutation	p.Lys210Glu(p.K210E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399640
Start	133475812:133475812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142623314
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399640
Start	133465953:133465953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769416956
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399640
Start	133461959:133461959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399640
Start	133459821:133459821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399640
Start	133461881:133461881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764268995
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ST3GAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133459784:133459784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Trp(p.R335W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399640
Start	133464790:133464790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671G>A
AA Mutation	p.Gly224Asp(p.G224D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399640
Start	133459920:133459920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript