Colon Cancer: Gene >> GALNT15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16175243:16175243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773183021
CDS Mutation	c.92C>T
AA Mutation	p.Ala31Val(p.A31V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16227466:16227466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756197962
CDS Mutation	c.1886G>A
AA Mutation	p.Arg629His(p.R629H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16195819:16195819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599A>G
AA Mutation	p.His200Arg(p.H200R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16208657:16208657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1066A>G
AA Mutation	p.Ile356Val(p.I356V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16195876:16195876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656C>A
AA Mutation	p.Pro219His(p.P219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16211204:16211204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142616039
CDS Mutation	c.1160C>T
AA Mutation	p.Ser387Leu(p.S387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16219525:16219525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515C>A
AA Mutation	p.Phe505Leu(p.F505L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339732
Start	16222653:16222653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339732
Start	16212619:16212619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339732
Start	16175571:16175571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34510233
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339732
Start	16200662:16200662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.754delG
AA Mutation	p.Val252Ter(p.V252*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000339732
Start	16219401:16219401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1393-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16175329:16175329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Asp60Asn(p.D60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16212686:16212686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191977190
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Cys(p.R439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16195845:16195845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625C>T
AA Mutation	p.Arg209Trp(p.R209W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339732
Start	16219446:16219446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436G>T
AA Mutation	p.Arg479Ile(p.R479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339732
Start	16175457:16175457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript