Colon Cancer: Gene >> GLYAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58710062:58710062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138125182
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Cys(p.R199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58712793:58712793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283C>G
AA Mutation	p.Leu95Val(p.L95V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58710687:58710687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200442404
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58709776:58709776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772239779
CDS Mutation	c.881T>C
AA Mutation	p.Val294Ala(p.V294A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58712855:58712855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221A>T
AA Mutation	p.Asn74Ile(p.N74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344743
Start	58709952:58709952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.705G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344743
Start	58715398:58715398(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.107delA
AA Mutation	p.Asn36ThrfsTer8(p.N36Tfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000344743
Start	58712853:58712854(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.222_223insCCTCTT
AA Mutation	p.Asn74_Thr75insProLeu(p.N74_T75insPL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GLYAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58710726:58710726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>A
AA Mutation	p.Leu118Ile(p.L118I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344743
Start	58712775:58712775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301C>A
AA Mutation	p.His101Asn(p.H101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344743
Start	58709919:58709919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>A
Mutation Classification	Silent
Feature Type	Transcript