Colon Cancer: Gene >> SEC23IP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119898694:119898694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431C>T
AA Mutation	p.Ala144Val(p.A144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119919551:119919551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980A>C
AA Mutation	p.Glu660Asp(p.E660D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119904200:119904200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024C>T
AA Mutation	p.Arg342Cys(p.R342C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119933722:119933722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2958A>C
AA Mutation	p.Glu986Asp(p.E986D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119933086:119933086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200302175
CDS Mutation	c.2840G>A
AA Mutation	p.Arg947Gln(p.R947Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119917854:119917854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119915812:119915812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145679618
CDS Mutation	c.1467C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119898653:119898653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201913734
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119904103:119904103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766134801
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000369075
Start	119933130:119933130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2884G>T
AA Mutation	p.Glu962Ter(p.E962*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000369075
Start	119915851:119915851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506G>A
AA Mutation	p.Trp502Ter(p.W502*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369075
Start	119926184:119926185(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2279_2280dupTG
AA Mutation	p.Asn761Ter(p.N761*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000369075
Start	119932132:119932132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2573-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SEC23IP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119904104:119904104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776224093
CDS Mutation	c.928G>A
AA Mutation	p.Val310Met(p.V310M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119930420:119930420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2561G>T
AA Mutation	p.Arg854Ile(p.R854I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript