Colon Cancer: Gene >> GALNT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132203664:132203664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6G>T
AA Mutation	p.Glu2Asp(p.E2D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132247936:132247936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782326537
CDS Mutation	c.1051G>A
AA Mutation	p.Gly351Ser(p.G351S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132203629:132203629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375048132
CDS Mutation	c.41G>A
AA Mutation	p.Arg14His(p.R14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132257846:132257846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132247989:132247989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782006018
CDS Mutation	c.998G>A
AA Mutation	p.Arg333His(p.R333H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132247980:132247980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007T>G
AA Mutation	p.Phe336Cys(p.F336C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132262525:132262525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781888420
CDS Mutation	c.520G>A
AA Mutation	p.Val174Met(p.V174M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132197234:132197234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374716980
CDS Mutation	c.587G>A
AA Mutation	p.Arg196Gln(p.R196Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132199218:132199218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775412981
CDS Mutation	c.355G>A
AA Mutation	p.Gly119Ser(p.G119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132201198:132201198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229C>A
AA Mutation	p.Arg77Ser(p.R77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132201198:132201198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769224342
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Cys(p.R77C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132199226:132199226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569920280
CDS Mutation	c.347C>T
AA Mutation	p.Ala116Val(p.A116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132197952:132197952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762383807
CDS Mutation	c.407G>A
AA Mutation	p.Arg136Gln(p.R136Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132260996:132260996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713C>T
AA Mutation	p.Ala238Val(p.A238V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397325
Start	132199216:132199216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200409792
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397325
Start	132201238:132201238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369565545
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328957
Start	132257868:132257868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369113640
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328957
Start	132262568:132262568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132197196:132197196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>T
AA Mutation	p.Asp209Tyr(p.D209Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397325
Start	132201215:132201215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767618128
CDS Mutation	c.212G>A
AA Mutation	p.Arg71His(p.R71H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328957
Start	132257705:132257705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782073701
CDS Mutation	c.943G>A
AA Mutation	p.Glu315Lys(p.E315K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript