Colon Cancer: Gene >> SEC16B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308284
Start	177933614:177933614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543330759
CDS Mutation	c.2594G>A
AA Mutation	p.Arg865Gln(p.R865Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308284
Start	177947929:177947929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762535664
CDS Mutation	c.1559A>C
AA Mutation	p.Lys520Thr(p.K520T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308284
Start	177954292:177954292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1450T>A
AA Mutation	p.Trp484Arg(p.W484R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308284
Start	177940643:177940643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308284
Start	177961624:177961624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308284
Start	177958876:177958876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369591529
CDS Mutation	c.1098G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308284
Start	177967693:177967693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308284
Start	177937322:177937322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2395delT
AA Mutation	p.Tyr799ThrfsTer17(p.Y799Tfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308284
Start	177958198:177958198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1299delC
AA Mutation	p.Ser434ValfsTer29(p.S434Vfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308284
Start	177958197:177958198(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs768388757
CDS Mutation	c.1299dupC
AA Mutation	p.Ser434GlnfsTer14(p.S434Qfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SEC16B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308284
Start	177937397:177937397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2320C>A
AA Mutation	p.Gln774Lys(p.Q774K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308284
Start	177958945:177958945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780402516
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript