Colon Cancer: Gene >> ZFHX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959962:72959962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756319969
CDS Mutation	c.184G>A
AA Mutation	p.Ala62Thr(p.A62T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959676:72959676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470G>T
AA Mutation	p.Cys157Phe(p.C157F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72950810:72950810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2875G>T
AA Mutation	p.Asp959Tyr(p.D959Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795481:72795481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7201A>C
AA Mutation	p.Thr2401Pro(p.T2401P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72798400:72798400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4282G>A
AA Mutation	p.Ala1428Thr(p.A1428T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72793347:72793347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9335C>A
AA Mutation	p.Pro3112His(p.P3112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72797059:72797059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5623G>A
AA Mutation	p.Glu1875Lys(p.E1875K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72798087:72798087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374743360
CDS Mutation	c.4595A>G
AA Mutation	p.Asn1532Ser(p.N1532S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959716:72959716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>A
AA Mutation	p.Val144Met(p.V144M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72797281:72797281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5401T>A
AA Mutation	p.Tyr1801Asn(p.Y1801N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72950518:72950518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745871900
CDS Mutation	c.3167G>A
AA Mutation	p.Arg1056Gln(p.R1056Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72798546:72798546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753592536
CDS Mutation	c.4136C>T
AA Mutation	p.Thr1379Met(p.T1379M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795240:72795240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7442C>T
AA Mutation	p.Pro2481Leu(p.P2481L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72794098:72794098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8584G>T
AA Mutation	p.Ala2862Ser(p.A2862S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959533:72959533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>A
AA Mutation	p.Gly205Arg(p.G205R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795996:72795996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6686C>A
AA Mutation	p.Pro2229His(p.P2229H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72787466:72787466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745550429
CDS Mutation	c.10810G>A
AA Mutation	p.Ala3604Thr(p.A3604T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72794125:72794125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200701402
CDS Mutation	c.8557G>A
AA Mutation	p.Ala2853Thr(p.A2853T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72796782:72796782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5900T>C
AA Mutation	p.Val1967Ala(p.V1967A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72788644:72788644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9632C>A
AA Mutation	p.Pro3211His(p.P3211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72788142:72788142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10134G>T
AA Mutation	p.Gln3378His(p.Q3378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959290:72959290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856T>A
AA Mutation	p.Leu286Met(p.L286M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72958077:72958077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2069T>C
AA Mutation	p.Met690Thr(p.M690T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959065:72959065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561634666
CDS Mutation	c.1081G>A
AA Mutation	p.Gly361Arg(p.G361R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72796855:72796855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5827A>G
AA Mutation	p.Asn1943Asp(p.N1943D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72794535:72794535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8147G>T
AA Mutation	p.Cys2716Phe(p.C2716F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72957577:72957577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146607776
CDS Mutation	c.2569G>A
AA Mutation	p.Ala857Thr(p.A857T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72787339:72787339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10937G>A
AA Mutation	p.Cys3646Tyr(p.C3646Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72958993:72958993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764687875
CDS Mutation	c.1153G>A
AA Mutation	p.Ala385Thr(p.A385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959838:72959838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776936617
CDS Mutation	c.308G>A
AA Mutation	p.Arg103His(p.R103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72788801:72788801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9475G>A
AA Mutation	p.Val3159Ile(p.V3159I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795015:72795015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147043604
CDS Mutation	c.7667C>T
AA Mutation	p.Ala2556Val(p.A2556V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72787639:72787639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10637A>G
AA Mutation	p.Gln3546Arg(p.Q3546R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72788296:72788296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9980T>C
AA Mutation	p.Leu3327Pro(p.L3327P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959262:72959262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754613484
CDS Mutation	c.884G>A
AA Mutation	p.Arg295His(p.R295H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959338:72959338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808G>A
AA Mutation	p.Asp270Asn(p.D270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72797489:72797489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144110473
CDS Mutation	c.5193G>T
AA Mutation	p.Gln1731His(p.Q1731H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72787820:72787820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10456T>C
AA Mutation	p.Ser3486Pro(p.S3486P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72957967:72957967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201721439
CDS Mutation	c.2179C>T
AA Mutation	p.Arg727Cys(p.R727C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795570:72795570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7112C>T
AA Mutation	p.Ala2371Val(p.A2371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72811945:72811945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760400785
CDS Mutation	c.3623C>T
AA Mutation	p.Ser1208Leu(p.S1208L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795860:72795860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6822A>T
AA Mutation	p.Gln2274His(p.Q2274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72797040:72797040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5642T>A
AA Mutation	p.Val1881Asp(p.V1881D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72811683:72811683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370933867
CDS Mutation	c.3758G>A
AA Mutation	p.Arg1253His(p.R1253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72794254:72794254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8428A>C
AA Mutation	p.Ile2810Leu(p.I2810L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795744:72795744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763494543
CDS Mutation	c.6938G>A
AA Mutation	p.Arg2313His(p.R2313H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72958128:72958128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2018G>T
AA Mutation	p.Cys673Phe(p.C673F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72794436:72794436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774192226
CDS Mutation	c.8246C>T
AA Mutation	p.Ala2749Val(p.A2749V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72788301:72788301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746288766
CDS Mutation	c.9975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72793631:72793631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9051G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72960041:72960041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72958229:72958229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527561596
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72795431:72795431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72794654:72794654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771903702
CDS Mutation	c.8028C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72959942:72959942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72795449:72795449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769762758
CDS Mutation	c.7233G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72796364:72796364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368070331
CDS Mutation	c.6318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	58
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72798476:72798476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4206C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	59
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72959591:72959591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747235758
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	60
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72795599:72795599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767177678
CDS Mutation	c.7083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	61
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72957437:72957437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150583300
CDS Mutation	c.2709G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	62
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72889840:72889840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	63
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72950550:72950550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3135T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	64
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72796712:72796712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5970G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	65
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72794534:72794534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8148C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	66
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72798185:72798185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4497G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	67
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72794759:72794759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148910628
CDS Mutation	c.7923C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	68
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72795302:72795302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748787751
CDS Mutation	c.7380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	69
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72793376:72793376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	70
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72950679:72950679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3006C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	71
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72788814:72788814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201412119
CDS Mutation	c.9462G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	72
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72795629:72795629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7053T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	73
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72950574:72950574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746294646
CDS Mutation	c.3111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	74
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72788622:72788622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9654G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	75
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72787851:72787851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759330286
CDS Mutation	c.10425C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	76
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72958805:72958805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148524035
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	77
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72787445:72787445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.10831delC
AA Mutation	p.His3611ThrfsTer83(p.H3611Tfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	78
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72811931:72811931(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3637delA
AA Mutation	p.Thr1213GlnfsTer31(p.T1213Qfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	79
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72788061:72788061(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.10215delC
AA Mutation	p.Ala3407LeufsTer78(p.A3407Lfs*78)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	80
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72797002:72797003(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5679_5680delGG
AA Mutation	p.Asp1894GlnfsTer34(p.D1894Qfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	81
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72788481:72788481(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.9795delC
AA Mutation	p.Thr3266ArgfsTer18(p.T3266Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	82
Mutation Consequence	stop_gained
Transcription ID	ENST00000268489
Start	72787172:72787172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11104A>T
AA Mutation	p.Arg3702Ter(p.R3702*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	83
Mutation Consequence	stop_gained
Transcription ID	ENST00000268489
Start	72959437:72959437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Ter(p.R237*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	84
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72957742:72957743(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2403dupA
AA Mutation	p.Pro802ThrfsTer9(p.P802Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	85
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72795215:72795216(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.7466dupC
AA Mutation	p.Pro2490SerfsTer44(p.P2490Sfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	86
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72957766:72957767(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2379dupC
AA Mutation	p.Ser794LeufsTer17(p.S794Lfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	87
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000268489
Start	72960196:72960196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-49-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	88
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000268489
Start	72797458:72797459(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs552138038
CDS Mutation	c.5221_5223dupCAA
AA Mutation	p.Gln1741dup(p.Q1741dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZFHX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72797361:72797361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5321C>A
AA Mutation	p.Pro1774His(p.P1774H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959517:72959517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>A
AA Mutation	p.Gly210Asp(p.G210D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959637:72959637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509T>C
AA Mutation	p.Phe170Ser(p.F170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72959904:72959904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242G>T
AA Mutation	p.Cys81Phe(p.C81F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72797070:72797070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5612G>A
AA Mutation	p.Ser1871Asn(p.S1871N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268489
Start	72795135:72795135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7547C>T
AA Mutation	p.Thr2516Ile(p.T2516I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72788829:72788829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9447G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72796181:72796181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367687288
CDS Mutation	c.6501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72959246:72959246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150869238
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268489
Start	72787968:72787968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368345791
CDS Mutation	c.10308G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72788687:72788687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.9589delC
AA Mutation	p.Gln3197SerfsTer44(p.Q3197Sfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268489
Start	72959782:72959783(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.363_364insT
AA Mutation	p.Glu122Ter(p.E122*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript