Colon Cancer: Gene >> F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46728685:46728685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320G>T
AA Mutation	p.Lys440Asn(p.K440N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46719725:46719725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144785536
CDS Mutation	c.103C>T
AA Mutation	p.Arg35Trp(p.R35W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46719240:46719240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775306348
CDS Mutation	c.5C>T
AA Mutation	p.Ala2Val(p.A2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46729384:46729384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477C>T
AA Mutation	p.Leu493Phe(p.L493F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000311907
Start	46729381:46729381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474T>G
AA Mutation	p.Leu492Val(p.L492V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46723189:46723189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326C>T
AA Mutation	p.Ala109Val(p.A109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46729391:46729391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1484C>T
AA Mutation	p.Ala495Val(p.A495V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46723204:46723204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760923326
CDS Mutation	c.341C>T
AA Mutation	p.Thr114Met(p.T114M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46726557:46726557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371085757
CDS Mutation	c.934G>A
AA Mutation	p.Glu312Lys(p.E312K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46723267:46723267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777785946
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46728672:46728672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436Gln(p.R436Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46726761:46726761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121918484
CDS Mutation	c.1054G>A
AA Mutation	p.Glu352Lys(p.E352K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46728122:46728122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257G>T
AA Mutation	p.Glu419Asp(p.E419D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46723485:46723485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752361229
CDS Mutation	c.526G>A
AA Mutation	p.Val176Met(p.V176M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311907
Start	46726130:46726130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758385055
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311907
Start	46726097:46726097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138260543
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311907
Start	46728032:46728032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1167G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311907
Start	46725872:46725872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311907
Start	46723454:46723454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311907
Start	46723409:46723409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371923575
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311907
Start	46719276:46719276(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.43delC
AA Mutation	p.Leu15TrpfsTer106(p.L15Wfs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000311907
Start	46739380:46739382(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1843_1845delAAG
AA Mutation	p.Lys615del(p.K615del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46728795:46728795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430A>C
AA Mutation	p.Tyr477Ser(p.Y477S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311907
Start	46739329:46739329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790A>G
AA Mutation	p.Asp597Gly(p.D597G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript