Colon Cancer: Gene >> F9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139530810:139530810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46A>G
AA Mutation	p.Thr16Ala(p.T16A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139530771:139530771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766259893
CDS Mutation	c.7C>T
AA Mutation	p.Arg3Cys(p.R3C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139560763:139560763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746A>C
AA Mutation	p.Asp249Ala(p.D249A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561870:139561870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185C>A
AA Mutation	p.Phe395Leu(p.F395L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139537086:139537086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165T>A
AA Mutation	p.Phe55Leu(p.F55L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561566:139561566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852249
CDS Mutation	c.881G>A
AA Mutation	p.Arg294Gln(p.R294Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561872:139561872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187G>A
AA Mutation	p.Cys396Tyr(p.C396Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139560786:139560786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200608775
CDS Mutation	c.769G>A
AA Mutation	p.Val257Ile(p.V257I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139537106:139537106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185G>T
AA Mutation	p.Arg62Ile(p.R62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561691:139561691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006A>C
AA Mutation	p.Ile336Leu(p.I336L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561827:139561827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Thr381Ile(p.T381I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561755:139561755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070G>T
AA Mutation	p.Gly357Val(p.G357V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218099
Start	139561654:139561654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528270752
CDS Mutation	c.969A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218099
Start	139560782:139560782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218099
Start	139551099:139551099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218099
Start	139548438:139548438(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.468delC
AA Mutation	p.Cys157ValfsTer46(p.C157Vfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000218099
Start	139561835:139561835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852261
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Ter(p.R384*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000218099
Start	139561547:139561547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862G>T
AA Mutation	p.Glu288Ter(p.E288*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218099
Start	139548411:139548412(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.440_441insGTACATGGAAC
AA Mutation	p.Asn147LysfsTer60(p.N147Kfs*60)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> F9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139561870:139561870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185C>A
AA Mutation	p.Phe395Leu(p.F395L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218099
Start	139541166:139541166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368T>C
AA Mutation	p.Phe123Ser(p.F123S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript