Colon Cancer: Gene >> FYCO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45936494:45936494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759599621
CDS Mutation	c.3994G>A
AA Mutation	p.Val1332Met(p.V1332M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45955364:45955364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748475750
CDS Mutation	c.3829G>A
AA Mutation	p.Asp1277Asn(p.D1277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45931117:45931117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4205G>A
AA Mutation	p.Ser1402Asn(p.S1402N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45966599:45966599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2735T>C
AA Mutation	p.Val912Ala(p.V912A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45931271:45931271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4051C>T
AA Mutation	p.Pro1351Ser(p.P1351S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45921820:45921820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4382T>G
AA Mutation	p.Phe1461Cys(p.F1461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45968282:45968282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052T>C
AA Mutation	p.Leu351Pro(p.L351P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45969703:45969703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602T>C
AA Mutation	p.Met201Thr(p.M201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45967585:45967585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1749G>T
AA Mutation	p.Glu583Asp(p.E583D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45967919:45967919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533441275
CDS Mutation	c.1415G>A
AA Mutation	p.Arg472Gln(p.R472Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45923678:45923678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4339A>G
AA Mutation	p.Ile1447Val(p.I1447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45968586:45968586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142017802
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Trp(p.R250W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45967952:45967952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382G>T
AA Mutation	p.Gly461Val(p.G461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45931241:45931241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149020169
CDS Mutation	c.4081G>A
AA Mutation	p.Gly1361Arg(p.G1361R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296137
Start	45923673:45923673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202242942
CDS Mutation	c.4344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296137
Start	45931251:45931251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373785569
CDS Mutation	c.4071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296137
Start	45967082:45967083(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2248_2251dupGAGA
AA Mutation	p.Lys751ArgfsTer12(p.K751Rfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FYCO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45975302:45975302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332C>T
AA Mutation	p.Ser111Phe(p.S111F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296137
Start	45967805:45967805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1529C>A
AA Mutation	p.Ser510Tyr(p.S510Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296137
Start	45973165:45973165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>A
Mutation Classification	Silent
Feature Type	Transcript