Colon Cancer: Gene >> SERPINI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295777
Start	167789174:167789174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46G>T
AA Mutation	p.Ala16Ser(p.A16S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295777
Start	167789370:167789370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242T>A
AA Mutation	p.Leu81Gln(p.L81Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295777
Start	167807317:167807317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955G>T
AA Mutation	p.Asp319Tyr(p.D319Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295777
Start	167807307:167807307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945T>G
AA Mutation	p.Ile315Met(p.I315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295777
Start	167794729:167794729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295777
Start	167789371:167789371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.248delA
AA Mutation	p.Asn83MetfsTer8(p.N83Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295777
Start	167790505:167790506(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.390dupA
AA Mutation	p.Tyr131IlefsTer3(p.Y131Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295777
Start	167825255:167825255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165C>A
AA Mutation	p.Leu389Ile(p.L389I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295777
Start	167790451:167790451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330T>G
AA Mutation	p.Asn110Lys(p.N110K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript