Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IGSF10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446036:151446036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3945A>C
AA Mutation p.Gln1315His(p.Q1315H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437353:151437353(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753363334
CDS Mutation c.7208G>A
AA Mutation p.Arg2403Gln(p.R2403Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151436975:151436975(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146905174
CDS Mutation c.7586G>A
AA Mutation p.Arg2529Gln(p.R2529Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437377:151437377(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7184C>A
AA Mutation p.Ser2395Tyr(p.S2395Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446445:151446445(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781278592
CDS Mutation c.3536C>T
AA Mutation p.Ser1179Leu(p.S1179L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151448587:151448587(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1394T>C
AA Mutation p.Met465Thr(p.M465T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000282466
Start 151457154:151457154(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.196T>A
AA Mutation p.Tyr66Asn(p.Y66N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151448402:151448402(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372867906
CDS Mutation c.1579C>T
AA Mutation p.Arg527Trp(p.R527W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447069:151447069(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2912C>T
AA Mutation p.Ser971Phe(p.S971F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445834:151445834(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372469513
CDS Mutation c.4147G>A
AA Mutation p.Glu1383Lys(p.E1383K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151453645:151453645(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.454C>T
AA Mutation p.Leu152Phe(p.L152F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437971:151437971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6590C>A
AA Mutation p.Ser2197Tyr(p.S2197Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151443173:151443173(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770046902
CDS Mutation c.5774C>T
AA Mutation p.Ser1925Leu(p.S1925L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445056:151445056(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4925G>T
AA Mutation p.Arg1642Met(p.R1642M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446886:151446886(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145119548
CDS Mutation c.3095G>A
AA Mutation p.Arg1032Gln(p.R1032Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437405:151437405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7156T>C
AA Mutation p.Tyr2386His(p.Y2386H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445072:151445072(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750424094
CDS Mutation c.4909T>C
AA Mutation p.Phe1637Leu(p.F1637L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447178:151447178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2803A>G
AA Mutation p.Met935Val(p.M935V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151443287:151443287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5660T>C
AA Mutation p.Leu1887Ser(p.L1887S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437594:151437594(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774302298
CDS Mutation c.6967G>A
AA Mutation p.Val2323Met(p.V2323M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151443548:151443548(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367812916
CDS Mutation c.5399C>T
AA Mutation p.Thr1800Met(p.T1800M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445325:151445325(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4656G>A
AA Mutation p.Met1552Ile(p.M1552I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151443740:151443740(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5207T>C
AA Mutation p.Val1736Ala(p.V1736A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151436948:151436948(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7613T>G
AA Mutation p.Ile2538Ser(p.I2538S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151453394:151453394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.705G>T
AA Mutation p.Gln235His(p.Q235H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447628:151447628(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2353C>G
AA Mutation p.Gln785Glu(p.Q785E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446967:151446967(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567335058
CDS Mutation c.3014C>T
AA Mutation p.Pro1005Leu(p.P1005L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447895:151447895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2086G>A
AA Mutation p.Ala696Thr(p.A696T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437170:151437170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7391T>G
AA Mutation p.Ile2464Ser(p.I2464S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437416:151437416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7145G>T
AA Mutation p.Gly2382Val(p.G2382V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151438302:151438302(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201909176
CDS Mutation c.6259G>A
AA Mutation p.Asp2087Asn(p.D2087N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445298:151445298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4683G>T
AA Mutation p.Gln1561His(p.Q1561H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447257:151447257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2724G>T
AA Mutation p.Gln908His(p.Q908H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151453391:151453391(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.708G>T
AA Mutation p.Glu236Asp(p.E236D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151458618:151458618(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374510873
CDS Mutation c.92G>A
AA Mutation p.Arg31His(p.R31H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447417:151447417(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2564A>G
AA Mutation p.Glu855Gly(p.E855G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151448115:151448115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1866G>T
AA Mutation p.Lys622Asn(p.K622N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446173:151446173(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749759395
CDS Mutation c.3808G>A
AA Mutation p.Ala1270Thr(p.A1270T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151448933:151448933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1048G>T
AA Mutation p.Asp350Tyr(p.D350Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446919:151446919(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs35114212
CDS Mutation c.3062G>A
AA Mutation p.Arg1021Gln(p.R1021Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151438574:151438574(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5987A>G
AA Mutation p.Tyr1996Cys(p.Y1996C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151437988:151437988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6573A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151446447:151446447(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3534A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151443793:151443793(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759777108
CDS Mutation c.5154C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151438117:151438117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6444A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151437055:151437055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7506A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151448274:151448274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1707A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151437634:151437634(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201962174
CDS Mutation c.6927C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151447038:151447038(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143010277
CDS Mutation c.2943G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151443409:151443409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5538G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151448787:151448787(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146034413
CDS Mutation c.1194G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151447977:151447977(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745895078
CDS Mutation c.2004G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151448739:151448739(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750357876
CDS Mutation c.1242T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151446833:151446833(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3148delA
AA Mutation p.Ser1050AlafsTer12(p.S1050Afs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151446921:151446921(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3060delG
AA Mutation p.Arg1021GlyfsTer41(p.R1021Gfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151445403:151445403(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4578delC
AA Mutation p.Lys1527ArgfsTer29(p.K1527Rfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151445782:151445782(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4199delA
AA Mutation p.Asn1400ThrfsTer18(p.N1400Tfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151438296:151438297(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.6264_6265insTGTTATAACTGTTA
AA Mutation p.Ser2089CysfsTer5(p.S2089Cfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151449177:151449178(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.803_804insAT
AA Mutation p.Leu269CysfsTer2(p.L269Cfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 60
Mutation Consequence frameshift_variant
Transcription ID ENST00000282466
Start 151449179:151449180(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.801_802insA
AA Mutation p.Pro268ThrfsTer18(p.P268Tfs*18)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 61
Mutation Consequence inframe_deletion
Transcription ID ENST00000282466
Start 151458697:151458705(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5_13delAGGTAAAAG
AA Mutation p.Lys2_Gly5delinsSer(p.K2_G5delinsS)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> IGSF10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151436975:151436975(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7586G>T
AA Mutation p.Arg2529Leu(p.R2529L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151438371:151438371(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768260632
CDS Mutation c.6190G>A
AA Mutation p.Gly2064Ser(p.G2064S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151458532:151458532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.178G>A
AA Mutation p.Glu60Lys(p.E60K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437830:151437830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6731G>T
AA Mutation p.Arg2244Ile(p.R2244I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151438277:151438277(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6284G>T
AA Mutation p.Arg2095Ile(p.R2095I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446082:151446082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3899G>T
AA Mutation p.Ser1300Ile(p.S1300I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151448830:151448830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1151C>T
AA Mutation p.Ser384Phe(p.S384F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151437818:151437818(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6743A>C
AA Mutation p.Lys2248Thr(p.K2248T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151443540:151443540(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5407G>A
AA Mutation p.Gly1803Arg(p.G1803R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151447365:151447365(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2616G>T
AA Mutation p.Lys872Asn(p.K872N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151443087:151443087(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5860A>C
AA Mutation p.Asn1954His(p.N1954H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445743:151445743(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4238G>T
AA Mutation p.Arg1413Ile(p.R1413I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151445917:151445917(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4064G>T
AA Mutation p.Arg1355Met(p.R1355M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151446406:151446406(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3575T>G
AA Mutation p.Ile1192Ser(p.I1192S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000282466
Start 151448614:151448614(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1367C>T
AA Mutation p.Ala456Val(p.A456V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151437259:151437259(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7302T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151438381:151438381(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761874663
CDS Mutation c.6180C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151447106:151447106(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2875A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000282466
Start 151449057:151449057(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.924T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence stop_gained
Transcription ID ENST00000282466
Start 151438539:151438539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6022G>T
AA Mutation p.Glu2008Ter(p.E2008*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript