Colon Cancer: Gene >> SERPINC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173904052:173904052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232G>T
AA Mutation	p.Gly411Val(p.G411V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173914894:173914894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67C>T
AA Mutation	p.Leu23Phe(p.L23F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173909775:173909775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>G
AA Mutation	p.Asp310Glu(p.D310E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173903927:173903927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357A>G
AA Mutation	p.Ile453Val(p.I453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173903989:173903989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295T>C
AA Mutation	p.Val432Ala(p.V432A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173914659:173914659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199895690
CDS Mutation	c.302C>T
AA Mutation	p.Ser101Phe(p.S101F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173909638:173909638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373515340
CDS Mutation	c.1067G>A
AA Mutation	p.Arg356His(p.R356H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173911884:173911884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539G>A
AA Mutation	p.Gly180Glu(p.G180E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367698
Start	173909924:173909924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781T>C
AA Mutation	p.Phe261Leu(p.F261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367698
Start	173909628:173909628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773134244
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367698
Start	173909715:173909715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990A>G
Mutation Classification	Silent
Feature Type	Transcript