Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FAT2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151525838:151525838(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10436C>A
AA Mutation p.Pro3479Gln(p.P3479Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521437:151521437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11156G>A
AA Mutation p.Arg3719Gln(p.R3719Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151549316:151549316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4768G>T
AA Mutation p.Val1590Phe(p.V1590F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151512290:151512290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11780C>G
AA Mutation p.Ala3927Gly(p.A3927G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151550628:151550628(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556459301
CDS Mutation c.4540C>T
AA Mutation p.Leu1514Phe(p.L1514F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151542945:151542945(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201629483
CDS Mutation c.8182C>T
AA Mutation p.Arg2728Trp(p.R2728W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151566014:151566014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137947267
CDS Mutation c.2918G>A
AA Mutation p.Arg973Gln(p.R973Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151531841:151531841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9557C>T
AA Mutation p.Thr3186Met(p.T3186M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543829:151543829(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772956088
CDS Mutation c.7298C>T
AA Mutation p.Ser2433Leu(p.S2433L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151531911:151531911(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141162743
CDS Mutation c.9487G>A
AA Mutation p.Asp3163Asn(p.D3163N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151542894:151542894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8233G>T
AA Mutation p.Asp2745Tyr(p.D2745Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543203:151543203(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7924G>A
AA Mutation p.Val2642Met(p.V2642M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567352:151567352(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1580G>T
AA Mutation p.Arg527Ile(p.R527I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568096:151568096(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.836C>T
AA Mutation p.Ala279Val(p.A279V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151566483:151566483(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138650496
CDS Mutation c.2449G>A
AA Mutation p.Ala817Thr(p.A817T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151517642:151517642(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11441A>G
AA Mutation p.Glu3814Gly(p.E3814G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151517714:151517714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11369C>T
AA Mutation p.Ala3790Val(p.A3790V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545573:151545573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5554G>A
AA Mutation p.Ala1852Thr(p.A1852T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151531604:151531604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9794G>A
AA Mutation p.Arg3265His(p.R3265H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545679:151545679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5448T>A
AA Mutation p.Asp1816Glu(p.D1816E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505638:151505638(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749529613
CDS Mutation c.12977G>A
AA Mutation p.Arg4326Gln(p.R4326Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151553218:151553218(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4115G>A
AA Mutation p.Ser1372Asn(p.S1372N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151546179:151546179(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145729602
CDS Mutation c.4948G>A
AA Mutation p.Val1650Ile(p.V1650I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151534453:151534453(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs553647582
CDS Mutation c.9383T>C
AA Mutation p.Val3128Ala(p.V3128A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544777:151544777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763727182
CDS Mutation c.6350G>A
AA Mutation p.Arg2117Gln(p.R2117Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544214:151544214(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200330283
CDS Mutation c.6913C>T
AA Mutation p.Arg2305Cys(p.R2305C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545477:151545477(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5650C>T
AA Mutation p.Pro1884Ser(p.P1884S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543418:151543418(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs560174924
CDS Mutation c.7709C>T
AA Mutation p.Thr2570Met(p.T2570M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505614:151505614(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13001C>T
AA Mutation p.Ser4334Phe(p.S4334F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544108:151544108(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7019A>T
AA Mutation p.Glu2340Val(p.E2340V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568159:151568159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758396931
CDS Mutation c.773C>T
AA Mutation p.Ser258Leu(p.S258L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545456:151545456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5671C>A
AA Mutation p.Leu1891Ile(p.L1891I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544220:151544220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201714112
CDS Mutation c.6907C>T
AA Mutation p.Arg2303Trp(p.R2303W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151566300:151566300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2632A>G
AA Mutation p.Thr878Ala(p.T878A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151540573:151540573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9033T>G
AA Mutation p.Cys3011Trp(p.C3011W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568199:151568199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.733C>T
AA Mutation p.His245Tyr(p.H245Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505585:151505585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13030T>C
AA Mutation p.Cys4344Arg(p.C4344R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151563565:151563565(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3334A>G
AA Mutation p.Arg1112Gly(p.R1112G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505890:151505890(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144888662
CDS Mutation c.12725G>A
AA Mutation p.Arg4242His(p.R4242H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568681:151568681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.251C>T
AA Mutation p.Thr84Ile(p.T84I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505921:151505921(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12694A>T
AA Mutation p.Met4232Leu(p.M4232L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521636:151521636(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10957A>T
AA Mutation p.Arg3653Trp(p.R3653W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151542581:151542581(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8546C>T
AA Mutation p.Ala2849Val(p.A2849V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568417:151568417(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.515C>T
AA Mutation p.Ala172Val(p.A172V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151563516:151563516(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs190882193
CDS Mutation c.3383C>T
AA Mutation p.Thr1128Met(p.T1128M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567576:151567576(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1356C>A
AA Mutation p.Asn452Lys(p.N452K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505923:151505923(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12692A>G
AA Mutation p.Glu4231Gly(p.E4231G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521594:151521594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10999C>A
AA Mutation p.His3667Asn(p.H3667N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151551522:151551522(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778228742
CDS Mutation c.4241C>T
AA Mutation p.Ser1414Leu(p.S1414L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567101:151567101(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1831G>T
AA Mutation p.Asp611Tyr(p.D611Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505714:151505714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12901C>T
AA Mutation p.Arg4301Cys(p.R4301C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545239:151545239(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5888A>G
AA Mutation p.Asp1963Gly(p.D1963G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151542350:151542350(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377736336
CDS Mutation c.8777C>T
AA Mutation p.Ala2926Val(p.A2926V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151537943:151537943(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9043C>A
AA Mutation p.Leu3015Ile(p.L3015I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151546318:151546318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4809C>G
AA Mutation p.Phe1603Leu(p.F1603L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151507475:151507475(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12196C>T
AA Mutation p.Leu4066Phe(p.L4066F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 57
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000261800
Start 151563639:151563639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3260G>A
AA Mutation p.Gly1087Glu(p.G1087E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 58
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545863:151545863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5264C>A
AA Mutation p.Ala1755Asp(p.A1755D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 59
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567187:151567187(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750724598
CDS Mutation c.1745C>T
AA Mutation p.Ser582Leu(p.S582L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 60
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568308:151568308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.624G>T
AA Mutation p.Lys208Asn(p.K208N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 61
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567794:151567794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377151192
CDS Mutation c.1138C>T
AA Mutation p.Arg380Cys(p.R380C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 62
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521829:151521829(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10764C>G
AA Mutation p.Ile3588Met(p.I3588M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 63
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151545557:151545557(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5570A>G
AA Mutation p.Gln1857Arg(p.Q1857R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 64
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521453:151521453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11140G>A
AA Mutation p.Val3714Met(p.V3714M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 65
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151567186:151567186(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765690558
CDS Mutation c.1746G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 66
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151565818:151565818(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3114G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 67
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151563575:151563575(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3324A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 68
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151543942:151543942(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7185A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 69
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151544608:151544608(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6519T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 70
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151565998:151565998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2934A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 71
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151567960:151567960(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747786056
CDS Mutation c.972G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 72
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151566907:151566907(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2025A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 73
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151542361:151542361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748256749
CDS Mutation c.8766C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 74
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151531645:151531645(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769890468
CDS Mutation c.9753C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 75
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151534578:151534578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9258G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 76
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151568332:151568332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201481988
CDS Mutation c.600C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 77
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151534485:151534485(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9351C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 78
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151566283:151566283(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373152684
CDS Mutation c.2649C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 79
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151531798:151531798(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756296108
CDS Mutation c.9600G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 80
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151525858:151525858(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10416C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 81
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151543228:151543228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7899C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 82
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151546069:151546069(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5058C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 83
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151568268:151568268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778690411
CDS Mutation c.664C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 84
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151563623:151563623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3276G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 85
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151507544:151507544(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.12127delG
AA Mutation p.Asp4043ThrfsTer8(p.D4043Tfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 86
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151505817:151505817(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.12798delC
AA Mutation p.Cys4267ValfsTer129(p.C4267Vfs*129)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 87
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151525891:151525891(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.10383delC
AA Mutation p.Tyr3462ThrfsTer16(p.Y3462Tfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 88
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151567463:151567463(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1469delA
AA Mutation p.Asn490MetfsTer36(p.N490Mfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 89
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151543997:151543997(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7130delC
AA Mutation p.Pro2377GlnfsTer41(p.P2377Qfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 90
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151521447:151521447(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.11146delG
AA Mutation p.Val3716PhefsTer44(p.V3716Ffs*44)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 91
Mutation Consequence stop_gained
Transcription ID ENST00000261800
Start 151554501:151554501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3806C>G
AA Mutation p.Ser1269Ter(p.S1269*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 92
Mutation Consequence stop_gained
Transcription ID ENST00000261800
Start 151544583:151544583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6544G>T
AA Mutation p.Glu2182Ter(p.E2182*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 93
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151567573:151567574(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1358_1359insTCCATTTTCC
AA Mutation p.His454ProfsTer14(p.H454Pfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FAT2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151531781:151531781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9617T>C
AA Mutation p.Val3206Ala(p.V3206A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151537822:151537822(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200557129
CDS Mutation c.9164C>T
AA Mutation p.Ala3055Val(p.A3055V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543817:151543817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7310C>T
AA Mutation p.Ser2437Phe(p.S2437F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567700:151567700(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748234388
CDS Mutation c.1232G>A
AA Mutation p.Arg411Gln(p.R411Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544522:151544522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6605G>A
AA Mutation p.Arg2202Gln(p.R2202Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151553342:151553342(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746994544
CDS Mutation c.3991C>T
AA Mutation p.Arg1331Trp(p.R1331W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567163:151567163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1769A>G
AA Mutation p.Asp590Gly(p.D590G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151566889:151566889(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2043G>T
AA Mutation p.Lys681Asn(p.K681N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151531908:151531908(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200687536
CDS Mutation c.9490G>A
AA Mutation p.Ala3164Thr(p.A3164T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151505859:151505859(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12756G>A
AA Mutation p.Met4252Ile(p.M4252I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151542435:151542435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8692G>T
AA Mutation p.Asp2898Tyr(p.D2898Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543846:151543846(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7281C>A
AA Mutation p.Phe2427Leu(p.F2427L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544829:151544829(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6298G>A
AA Mutation p.Gly2100Arg(p.G2100R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151554581:151554581(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3726C>A
AA Mutation p.Phe1242Leu(p.F1242L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151566120:151566120(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2812C>A
AA Mutation p.Leu938Met(p.L938M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568820:151568820(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.112T>C
AA Mutation p.Tyr38His(p.Y38H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151568006:151568006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.926G>A
AA Mutation p.Ser309Asn(p.S309N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151543198:151543198(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7929C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151566811:151566811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2121T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151542349:151542349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374640362
CDS Mutation c.8778G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151545663:151545663(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749649560
CDS Mutation c.5464C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151521454:151521454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11139A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151531915:151531915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9483C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151543732:151543732(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7395G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151568374:151568374(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.558C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151545958:151545958(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5169C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151568884:151568884(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752118764
CDS Mutation c.48G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence stop_gained
Transcription ID ENST00000261800
Start 151543995:151543995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7132G>T
AA Mutation p.Glu2378Ter(p.E2378*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000261800
Start 151545260:151545261(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.5866dupA
AA Mutation p.Ile1956AsnfsTer8(p.I1956Nfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript