Colon Cancer: Gene >> UNC5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71286857:71286857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201690824
CDS Mutation	c.721G>A
AA Mutation	p.Val241Ile(p.V241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71286783:71286783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753995814
CDS Mutation	c.647G>A
AA Mutation	p.Arg216His(p.R216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71288636:71288636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763454665
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Cys(p.R324C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71288583:71288583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780005887
CDS Mutation	c.917C>T
AA Mutation	p.Thr306Met(p.T306M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71290993:71290993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178C>T
AA Mutation	p.Ala393Val(p.A393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71291677:71291677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202076199
CDS Mutation	c.1540G>A
AA Mutation	p.Asp514Asn(p.D514N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71287720:71287720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781171880
CDS Mutation	c.856G>A
AA Mutation	p.Glu286Lys(p.E286K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71288973:71288973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082G>A
AA Mutation	p.Ser361Asn(p.S361N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71290936:71290936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766271403
CDS Mutation	c.1121C>T
AA Mutation	p.Ala374Val(p.A374V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71286840:71286840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764122864
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71296686:71296686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370153366
CDS Mutation	c.2434G>A
AA Mutation	p.Val812Met(p.V812M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71291569:71291569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432C>T
AA Mutation	p.Pro478Ser(p.P478S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71291606:71291606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543519250
CDS Mutation	c.1469C>T
AA Mutation	p.Thr490Met(p.T490M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71285407:71285407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530C>T
AA Mutation	p.Pro177Leu(p.P177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71291725:71291725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761845735
CDS Mutation	c.1588G>A
AA Mutation	p.Gly530Ser(p.G530S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71291486:71291486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1349G>A
AA Mutation	p.Gly450Asp(p.G450D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71285366:71285366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71287605:71287605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140557574
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71291709:71291709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774021056
CDS Mutation	c.1572G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71284754:71284754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374918405
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71285408:71285408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202141876
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71292516:71292516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770825448
CDS Mutation	c.1734C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71299262:71299262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368414601
CDS Mutation	c.2823C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71288578:71288578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758450668
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UNC5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335350
Start	71279910:71279910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747312686
CDS Mutation	c.169G>A
AA Mutation	p.Ala57Thr(p.A57T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71291775:71291775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374710244
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335350
Start	71291484:71291484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762531117
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript