Colon Cancer: Gene >> UNC5D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35549295:35549295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107C>G
AA Mutation	p.Thr36Ser(p.T36S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35568218:35568218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>T
AA Mutation	p.Arg148Met(p.R148M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35705940:35705940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>A
AA Mutation	p.Leu366Ile(p.L366I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35722359:35722359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267G>T
AA Mutation	p.Gly423Cys(p.G423C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35549412:35549412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>C
AA Mutation	p.Cys75Ser(p.C75S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35686638:35686638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013G>T
AA Mutation	p.Arg338Ile(p.R338I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35759414:35759414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2258C>T
AA Mutation	p.Ser753Phe(p.S753F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35766913:35766913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2325C>A
AA Mutation	p.Phe775Leu(p.F775L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35790363:35790363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2662T>G
AA Mutation	p.Leu888Val(p.L888V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35686635:35686635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010C>T
AA Mutation	p.Pro337Leu(p.P337L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35684632:35684632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802T>A
AA Mutation	p.Cys268Ser(p.C268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35726519:35726519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671G>A
AA Mutation	p.Met557Ile(p.M557I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35748589:35748589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1829T>C
AA Mutation	p.Met610Thr(p.M610T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35774326:35774326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763472547
CDS Mutation	c.2506G>A
AA Mutation	p.Ala836Thr(p.A836T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35790417:35790417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2716G>A
AA Mutation	p.Glu906Lys(p.E906K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35750759:35750759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2113G>A
AA Mutation	p.Asp705Asn(p.D705N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35774468:35774468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2648G>A
AA Mutation	p.Ser883Asn(p.S883N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35705933:35705933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089A>C
AA Mutation	p.Lys363Asn(p.K363N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35731074:35731074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744T>C
AA Mutation	p.Ser582Pro(p.S582P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35726183:35726183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35748623:35748623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142826516
CDS Mutation	c.1863G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35750641:35750641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145027081
CDS Mutation	c.1995G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35683708:35683708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780881731
CDS Mutation	c.732G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35759361:35759361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2205G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35549305:35549305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761905222
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000404895
Start	35686670:35686670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045C>T
AA Mutation	p.Gln349Ter(p.Q349*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000404895
Start	35549360:35549360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>T
AA Mutation	p.Glu58Ter(p.E58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000404895
Start	35748652:35748652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1892G>A
AA Mutation	p.Trp631Ter(p.W631*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UNC5D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35790477:35790477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2776G>C
AA Mutation	p.Gly926Arg(p.G926R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35774399:35774399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773478021
CDS Mutation	c.2579G>A
AA Mutation	p.Arg860Gln(p.R860Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35684618:35684618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788C>G
AA Mutation	p.Ala263Gly(p.A263G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404895
Start	35766918:35766918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2330G>A
AA Mutation	p.Arg777His(p.R777H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35549452:35549452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763941864
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35722226:35722226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188758803
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404895
Start	35726507:35726507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659G>A
Mutation Classification	Silent
Feature Type	Transcript