Colon Cancer: Gene >> GALNT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4763958:4763958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747668034
CDS Mutation	c.1504A>C
AA Mutation	p.Asn502His(p.N502H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4763275:4763275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382A>T
AA Mutation	p.Asp461Val(p.D461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4726606:4726606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754440838
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4761051:4761051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766726075
CDS Mutation	c.1267G>A
AA Mutation	p.Ala423Thr(p.A423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4726808:4726808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488T>C
AA Mutation	p.Ile163Thr(p.I163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4765473:4765473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688C>T
AA Mutation	p.Ala563Val(p.A563V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4745464:4745464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200878740
CDS Mutation	c.896G>A
AA Mutation	p.Arg299His(p.R299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252318
Start	4761050:4761050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140072173
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252318
Start	4726707:4726707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143654718
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252318
Start	4720773:4720773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252318
Start	4720703:4720703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26A>G
AA Mutation	p.Lys9Arg(p.K9R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript