Colon Cancer: Gene >> ST6GALNAC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76574446:76574446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548481942
CDS Mutation	c.280G>A
AA Mutation	p.Gly94Arg(p.G94R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76574415:76574415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776553153
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76572759:76572759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547A>G
AA Mutation	p.Ile183Val(p.I183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76570632:76570632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763902940
CDS Mutation	c.706G>A
AA Mutation	p.Asp236Asn(p.D236N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76573358:76573358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138357790
CDS Mutation	c.367G>A
AA Mutation	p.Ala123Thr(p.A123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76573307:76573307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>T
AA Mutation	p.Pro140Ser(p.P140S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76567461:76567461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949T>C
AA Mutation	p.Cys317Arg(p.C317R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225276
Start	76578783:76578783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225276
Start	76570633:76570633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141795987
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225276
Start	76567519:76567519(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.891delT
AA Mutation	p.Phe297LeufsTer15(p.F297Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000225276
Start	76572693:76572693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613A>T
AA Mutation	p.Lys205Ter(p.K205*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ST6GALNAC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225276
Start	76566231:76566231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998T>G
AA Mutation	p.Phe333Cys(p.F333C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript