Colon Cancer: Gene >> ATF6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32115864:32115864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987C>T
AA Mutation	p.Pro663Ser(p.P663S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32115857:32115857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372075542
CDS Mutation	c.1994C>T
AA Mutation	p.Ser665Leu(p.S665L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32128155:32128155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53C>T
AA Mutation	p.Thr18Ile(p.T18I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32119086:32119086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022A>G
AA Mutation	p.Gln341Arg(p.Q341R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32119934:32119934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Gly286Ser(p.G286S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32117082:32117082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1640C>T
AA Mutation	p.Pro547Leu(p.P547L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375203
Start	32117637:32117637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482G>C
AA Mutation	p.Gln494His(p.Q494H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375203
Start	32118783:32118783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375203
Start	32128199:32128199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375203
Start	32119863:32119863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765381562
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375203
Start	32115859:32115859(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1992delC
AA Mutation	p.Ser665ArgfsTer46(p.S665Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000375203
Start	32119023:32119024(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1084_1085insTCTCAC
AA Mutation	p.Ala362delinsValSerPro(p.A362delinsVSP)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ATF6B

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000375203
Start	32121056:32121056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633G>A
AA Mutation	p.Trp211Ter(p.W211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript