Colon Cancer: Gene >> TRAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70583253:70583253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766963451
CDS Mutation	c.962G>A
AA Mutation	p.Arg321Gln(p.R321Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70587115:70587115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632A>C
AA Mutation	p.Tyr211Ser(p.Y211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70583790:70583790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750T>G
AA Mutation	p.Phe250Leu(p.F250L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70587166:70587166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581C>A
AA Mutation	p.Pro194His(p.P194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70586918:70586918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723T>A
AA Mutation	p.Phe241Leu(p.F241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70586920:70586920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721T>A
AA Mutation	p.Phe241Ile(p.F241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262213
Start	70608160:70608160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262213
Start	70574947:70574947(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1110delA
AA Mutation	p.Glu371ArgfsTer8(p.E371Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70574937:70574937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120T>C
AA Mutation	p.Ser374Pro(p.S374P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70583266:70583266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949A>C
AA Mutation	p.Asn317His(p.N317H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262213
Start	70586947:70586947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>A
AA Mutation	p.Leu232Ile(p.L232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262213
Start	70608094:70608094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106C>T
Mutation Classification	Silent
Feature Type	Transcript