Colon Cancer: Gene >> SCML4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107705310:107705310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135G>A
AA Mutation	p.Ala379Thr(p.A379T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107749807:107749807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163T>C
AA Mutation	p.Ser55Pro(p.S55P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107749804:107749804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748183780
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Trp(p.R56W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107746803:107746803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373G>A
AA Mutation	p.Glu125Lys(p.E125K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107772296:107772296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32G>A
AA Mutation	p.Arg11Gln(p.R11Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107720870:107720870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806G>A
AA Mutation	p.Cys269Tyr(p.C269Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107772308:107772308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184505614
CDS Mutation	c.20C>T
AA Mutation	p.Pro7Leu(p.P7L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107745069:107745069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562T>C
AA Mutation	p.Phe188Leu(p.F188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369020
Start	107772286:107772286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369020
Start	107707989:107707989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530348685
CDS Mutation	c.996G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369020
Start	107746723:107746723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369020
Start	107746855:107746855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SCML4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107720873:107720873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803A>G
AA Mutation	p.Tyr268Cys(p.Y268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107720822:107720822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>T
AA Mutation	p.Ala285Val(p.A285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107745050:107745050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555376188
CDS Mutation	c.581G>A
AA Mutation	p.Arg194Gln(p.R194Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369020
Start	107720804:107720804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769590136
CDS Mutation	c.872G>A
AA Mutation	p.Arg291His(p.R291H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369020
Start	107720917:107720917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759C>A
Mutation Classification	Silent
Feature Type	Transcript