Colon Cancer: Gene >> ENC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634811:74634811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675G>A
AA Mutation	p.Asp559Asn(p.D559N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635083:74635083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403G>A
AA Mutation	p.Cys468Tyr(p.C468Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635038:74635038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483His(p.R483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634904:74634904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1582C>T
AA Mutation	p.Arg528Cys(p.R528C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74636308:74636308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178C>T
AA Mutation	p.His60Tyr(p.H60Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635680:74635680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806C>T
AA Mutation	p.Ala269Val(p.A269V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635027:74635027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459G>A
AA Mutation	p.Ala487Thr(p.A487T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74636172:74636172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314C>T
AA Mutation	p.Ala105Val(p.A105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635491:74635491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.995A>G
AA Mutation	p.Glu332Gly(p.E332G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74636329:74636329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Gly53Arg(p.G53R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634802:74634802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684T>G
AA Mutation	p.Leu562Val(p.L562V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634750:74634750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736C>T
AA Mutation	p.Ala579Val(p.A579V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634765:74634765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758188798
CDS Mutation	c.1721C>T
AA Mutation	p.Ser574Leu(p.S574L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635302:74635302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184G>T
AA Mutation	p.Gly395Val(p.G395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635620:74635620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866G>A
AA Mutation	p.Arg289Gln(p.R289Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635794:74635794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692A>C
AA Mutation	p.Glu231Ala(p.E231A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634894:74634894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1592G>A
AA Mutation	p.Cys531Tyr(p.C531Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635254:74635254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232T>A
AA Mutation	p.Leu411Gln(p.L411Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302351
Start	74634770:74634770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777609813
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302351
Start	74634950:74634950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302351
Start	74635445:74635445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1041delG
AA Mutation	p.Arg348GlyfsTer39(p.R348Gfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302351
Start	74634990:74634990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1496delG
AA Mutation	p.Gly499ValfsTer26(p.G499Vfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302351
Start	74635439:74635439(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1047delG
AA Mutation	p.Ser350LeufsTer37(p.S350Lfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ENC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635812:74635812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674G>C
AA Mutation	p.Arg225Pro(p.R225P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635851:74635851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635A>G
AA Mutation	p.Glu212Gly(p.E212G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74635476:74635476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778976207
CDS Mutation	c.1010C>T
AA Mutation	p.Ala337Val(p.A337V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302351
Start	74634977:74634977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509C>A
AA Mutation	p.Phe503Leu(p.F503L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript