Colon Cancer: Gene >> ATF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161781967:161781967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215A>G
AA Mutation	p.Asp72Gly(p.D72G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367942
Start	161819818:161819818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095G>T
AA Mutation	p.Glu365Asp(p.E365D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161792237:161792237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>A
AA Mutation	p.Ala200Thr(p.A200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161853256:161853256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1466G>A
AA Mutation	p.Arg489Lys(p.R489K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367942
Start	161778319:161778319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158A>T
AA Mutation	p.Tyr53Phe(p.Y53F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161781994:161781994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242G>A
AA Mutation	p.Cys81Tyr(p.C81Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161958622:161958622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566071406
CDS Mutation	c.1981G>A
AA Mutation	p.Val661Ile(p.V661I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161792142:161792142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503A>C
AA Mutation	p.Lys168Thr(p.K168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161819668:161819668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945A>C
AA Mutation	p.Lys315Asn(p.K315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367942
Start	161958516:161958516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367942
Start	161802059:161802059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367942
Start	161819665:161819665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.947delA
AA Mutation	p.Asn316IlefsTer17(p.N316Ifs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367942
Start	161766362:161766363(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.7dupG
AA Mutation	p.Glu3GlyfsTer14(p.E3Gfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ATF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161784058:161784058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150872316
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Trp(p.R106W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367942
Start	161958533:161958533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771212825
CDS Mutation	c.1892C>T
AA Mutation	p.Ser631Leu(p.S631L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367942
Start	161781912:161781912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript