Colon Cancer: Gene >> CHST10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100398060:100398060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572773940
CDS Mutation	c.275G>T
AA Mutation	p.Cys92Phe(p.C92F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100398033:100398033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302C>T
AA Mutation	p.Ser101Leu(p.S101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393298:100393298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147487716
CDS Mutation	c.1018G>A
AA Mutation	p.Glu340Lys(p.E340K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100406599:100406599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148953500
CDS Mutation	c.77C>T
AA Mutation	p.Thr26Met(p.T26M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100397971:100397971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364C>A
AA Mutation	p.Leu122Ile(p.L122I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393723:100393723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593C>A
AA Mutation	p.Ala198Glu(p.A198E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393631:100393631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756646964
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393574:100393574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742A>T
AA Mutation	p.Asn248Tyr(p.N248Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100402646:100402646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110C>T
AA Mutation	p.Ala37Val(p.A37V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393262:100393262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>A
AA Mutation	p.Asp352Asn(p.D352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393739:100393739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764927277
CDS Mutation	c.577G>A
AA Mutation	p.Glu193Lys(p.E193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100395554:100395554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488G>A
AA Mutation	p.Gly163Asp(p.G163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264249
Start	100393521:100393521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3748933
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264249
Start	100393319:100393319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370119165
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Ter(p.R333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CHST10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393748:100393748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>T
AA Mutation	p.Asp190Tyr(p.D190Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100393387:100393387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367887748
CDS Mutation	c.929C>T
AA Mutation	p.Pro310Leu(p.P310L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264249
Start	100395520:100395520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522A>C
AA Mutation	p.Glu174Asp(p.E174D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264249
Start	100398041:100398041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377559099
CDS Mutation	c.294G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264249
Start	100393467:100393467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript