Colon Cancer: Gene >> ST8SIA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17331508:17331508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422T>A
AA Mutation	p.Val141Asp(p.V141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17327071:17327071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578G>A
AA Mutation	p.Gly193Glu(p.G193E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17390579:17390579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242G>A
AA Mutation	p.Cys81Tyr(p.C81Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17321317:17321317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758T>C
AA Mutation	p.Leu253Pro(p.L253P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17321201:17321201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>T
AA Mutation	p.Ala292Ser(p.A292S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377602
Start	17321214:17321214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141961243
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377602
Start	17327028:17327028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754645226
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377602
Start	17331468:17331468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377694286
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377602
Start	17321322:17321322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.753delA
AA Mutation	p.Ala252ProfsTer53(p.A252Pfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377602
Start	17453615:17453615(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.144delC
AA Mutation	p.Ala49GlnfsTer3(p.A49Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000377602
Start	17359530:17359530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Glu121Ter(p.E121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000377602
Start	17320952:17320952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123G>T
AA Mutation	p.Glu375Ter(p.E375*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ST8SIA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17327027:17327027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Asp208Asn(p.D208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377602
Start	17321116:17321116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765868275
CDS Mutation	c.959G>A
AA Mutation	p.Arg320His(p.R320H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377602
Start	17390536:17390536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753810111
CDS Mutation	c.285G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377602
Start	17321322:17321322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.753delA
AA Mutation	p.Ala252ProfsTer53(p.A252Pfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000377602
Start	17320952:17320952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123G>T
AA Mutation	p.Glu375Ter(p.E375*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript