Colon Cancer: Gene >> GCNT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75028939:75028939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770022108
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Cys(p.R367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029243:75029243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>A
AA Mutation	p.Phe265Leu(p.F265L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75028938:75028938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745887897
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367His(p.R367H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75028956:75028956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082A>G
AA Mutation	p.Asp361Gly(p.D361G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029221:75029221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138374806
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Trp(p.R273W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029994:75029994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44A>C
AA Mutation	p.Lys15Thr(p.K15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029761:75029761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277A>T
AA Mutation	p.Arg93Trp(p.R93W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029958:75029958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>T
AA Mutation	p.Ser27Phe(p.S27F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029631:75029631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407C>T
AA Mutation	p.Ser136Phe(p.S136F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029479:75029479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559T>G
AA Mutation	p.Phe187Val(p.F187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322348
Start	75029243:75029243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144350055
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322348
Start	75028781:75028781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322348
Start	75029158:75029158(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.880delC
AA Mutation	p.His294IlefsTer14(p.H294Ifs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000322348
Start	75029967:75029967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71G>A
AA Mutation	p.Trp24Ter(p.W24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322348
Start	75029157:75029158(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs768450027
CDS Mutation	c.880dupC
AA Mutation	p.His294ProfsTer2(p.H294Pfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GCNT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029542:75029542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774430078
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75029977:75029977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61T>G
AA Mutation	p.Leu21Val(p.L21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322348
Start	75028904:75028904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>A
AA Mutation	p.Phe378Leu(p.F378L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322348
Start	75028781:75028781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257C>A
Mutation Classification	Silent
Feature Type	Transcript