Colon Cancer: Gene >> SERPIND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215727
Start	20779676:20779676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Trp(p.R122W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215727
Start	20779623:20779623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311C>G
AA Mutation	p.Thr104Arg(p.T104R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215727
Start	20779587:20779587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275A>G
AA Mutation	p.Tyr92Cys(p.Y92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215727
Start	20783987:20783987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905A>C
AA Mutation	p.Lys302Thr(p.K302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000215727
Start	20786029:20786029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189T>A
AA Mutation	p.Phe397Ile(p.F397I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215727
Start	20779363:20779363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139081149
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215727
Start	20784081:20784081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1008257
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215727
Start	20779691:20779691(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.380delA
AA Mutation	p.Asn127ThrfsTer15(p.N127Tfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SERPIND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215727
Start	20779370:20779370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>A
AA Mutation	p.Gly20Arg(p.G20R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript