Colon Cancer: Gene >> CHST6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75478739:75478739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>A
AA Mutation	p.Glu364Lys(p.E364K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479668:75479668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Ser54Phe(p.S54F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479318:75479318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>A
AA Mutation	p.Val171Met(p.V171M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75478970:75478970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.859C>G
AA Mutation	p.Leu287Val(p.L287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479792:75479792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>A
AA Mutation	p.Ala13Thr(p.A13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479768:75479768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>A
AA Mutation	p.Leu21Ile(p.L21I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75478964:75478964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>A
AA Mutation	p.Ala289Thr(p.A289T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479077:75479077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752G>A
AA Mutation	p.Arg251His(p.R251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479513:75479513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>A
AA Mutation	p.Val106Met(p.V106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75478798:75478798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344His(p.R344H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332272
Start	75478989:75478989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332272
Start	75478827:75478827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHST6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332272
Start	75479459:75479459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332272
Start	75479670:75479670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766289401
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript