Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> VCAN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83579988:83579988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9889G>A
AA Mutation p.Gly3297Ser(p.G3297S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83519720:83519720(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1414G>A
AA Mutation p.Asp472Asn(p.D472N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83520885:83520885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2579G>T
AA Mutation p.Ser860Ile(p.S860I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538290:83538290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5287A>G
AA Mutation p.Thr1763Ala(p.T1763A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539955:83539955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6952A>G
AA Mutation p.Thr2318Ala(p.T2318A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540531:83540531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7528G>T
AA Mutation p.Val2510Leu(p.V2510L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540698:83540698(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7695A>C
AA Mutation p.Glu2565Asp(p.E2565D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83553430:83553430(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373863261
CDS Mutation c.9560G>A
AA Mutation p.Arg3187Gln(p.R3187Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83545632:83545632(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9361G>A
AA Mutation p.Gly3121Arg(p.G3121R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83520405:83520405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2099C>T
AA Mutation p.Thr700Ile(p.T700I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83490236:83490236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.209A>G
AA Mutation p.Glu70Gly(p.E70G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521680:83521680(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146606609
CDS Mutation c.3374G>A
AA Mutation p.Arg1125His(p.R1125H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539530:83539530(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6527C>A
AA Mutation p.Ser2176Tyr(p.S2176Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83537332:83537332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4329C>A
AA Mutation p.Phe1443Leu(p.F1443L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83542265:83542265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9262C>A
AA Mutation p.Pro3088Thr(p.P3088T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538768:83538768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5765G>T
AA Mutation p.Arg1922Met(p.R1922M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521174:83521174(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2868T>G
AA Mutation p.Ser956Arg(p.S956R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539470:83539470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6467C>A
AA Mutation p.Ser2156Tyr(p.S2156Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541594:83541594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8591C>A
AA Mutation p.Ser2864Tyr(p.S2864Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83547974:83547974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9383T>G
AA Mutation p.Phe3128Cys(p.F3128C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83522148:83522148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs570361402
CDS Mutation c.3842C>T
AA Mutation p.Thr1281Met(p.T1281M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83520216:83520216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1910G>C
AA Mutation p.Gly637Ala(p.G637A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83580112:83580112(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754880024
CDS Mutation c.10013G>A
AA Mutation p.Arg3338Gln(p.R3338Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83537193:83537193(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4190C>A
AA Mutation p.Ala1397Glu(p.A1397E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83512327:83512327(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.973C>A
AA Mutation p.Leu325Met(p.L325M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83483539:83483539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.21C>G
AA Mutation p.Ser7Arg(p.S7R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83537854:83537854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4851A>C
AA Mutation p.Glu1617Asp(p.E1617D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541407:83541407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8404T>A
AA Mutation p.Ser2802Thr(p.S2802T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539068:83539068(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6065T>A
AA Mutation p.Val2022Asp(p.V2022D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540061:83540061(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200015194
CDS Mutation c.7058C>T
AA Mutation p.Thr2353Met(p.T2353M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83493879:83493879(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.696C>A
AA Mutation p.Phe232Leu(p.F232L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83537772:83537772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4769C>A
AA Mutation p.Ser1590Tyr(p.S1590Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83512222:83512222(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.868G>A
AA Mutation p.Gly290Ser(p.G290S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541455:83541455(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8452G>A
AA Mutation p.Ala2818Thr(p.A2818T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83554980:83554980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9677T>A
AA Mutation p.Ile3226Lys(p.I3226K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83522232:83522232(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149651541
CDS Mutation c.3926C>T
AA Mutation p.Thr1309Met(p.T1309M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83520093:83520093(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1787A>G
AA Mutation p.Asp596Gly(p.D596G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521295:83521295(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2989C>A
AA Mutation p.Leu997Ile(p.L997I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541794:83541794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8791G>T
AA Mutation p.Asp2931Tyr(p.D2931Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83542115:83542115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9112C>A
AA Mutation p.Leu3038Ile(p.L3038I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540417:83540417(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7414C>T
AA Mutation p.Pro2472Ser(p.P2472S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265077
Start 83579982:83579982(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9883G>A
AA Mutation p.Ala3295Thr(p.A3295T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83580111:83580111(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10012C>T
AA Mutation p.Arg3338Trp(p.R3338W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83483580:83483580(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.62T>C
AA Mutation p.Leu21Pro(p.L21P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83490214:83490214(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.187C>T
AA Mutation p.Arg63Cys(p.R63C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540216:83540216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7213G>A
AA Mutation p.Ala2405Thr(p.A2405T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541624:83541624(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147798761
CDS Mutation c.8621C>T
AA Mutation p.Ala2874Val(p.A2874V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83580040:83580040(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763390705
CDS Mutation c.9941G>A
AA Mutation p.Arg3314His(p.R3314H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83545570:83545570(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9299A>G
AA Mutation p.Asn3100Ser(p.N3100S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539856:83539856(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6853C>A
AA Mutation p.Pro2285Thr(p.P2285T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521173:83521173(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2867G>C
AA Mutation p.Ser956Thr(p.S956T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521932:83521932(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3626C>T
AA Mutation p.Thr1209Ile(p.T1209I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540510:83540510(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7507A>G
AA Mutation p.Thr2503Ala(p.T2503A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83520553:83520553(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2247C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83539858:83539858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6855C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83490460:83490460(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.433C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83539660:83539660(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6657A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83537197:83537197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4194T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83545562:83545562(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375652154
CDS Mutation c.9291G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83537461:83537461(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774610543
CDS Mutation c.4458C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83572421:83572421(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374136117
CDS Mutation c.9741C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83490429:83490429(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs558279284
CDS Mutation c.402C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83522014:83522014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367818886
CDS Mutation c.3708C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 64
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83540422:83540422(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61754536
CDS Mutation c.7419C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 65
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83572487:83572487(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9807T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 66
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83539963:83539963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6960C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 67
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83537152:83537152(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4149A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 68
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83540446:83540446(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7443A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 69
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83519503:83519503(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1197A>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 70
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83579987:83579987(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758458805
CDS Mutation c.9888C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 71
Mutation Consequence frameshift_variant
Transcription ID ENST00000265077
Start 83519495:83519495(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1191delC
AA Mutation p.Val398TrpfsTer22(p.V398Wfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 72
Mutation Consequence stop_gained
Transcription ID ENST00000265077
Start 83540483:83540483(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7480G>T
AA Mutation p.Glu2494Ter(p.E2494*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 73
Mutation Consequence stop_gained
Transcription ID ENST00000265077
Start 83538536:83538536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5533G>T
AA Mutation p.Glu1845Ter(p.E1845*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 74
Mutation Consequence frameshift_variant
Transcription ID ENST00000265077
Start 83540290:83540291(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.7289dupG
AA Mutation p.Glu2431ArgfsTer10(p.E2431Rfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 75
Mutation Consequence splice_donor_variant
Transcription ID ENST00000265077
Start 83580163:83580163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10063+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> VCAN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83519943:83519943(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1637G>A
AA Mutation p.Gly546Asp(p.G546D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83493901:83493901(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.718G>A
AA Mutation p.Asp240Asn(p.D240N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539494:83539494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6491A>G
AA Mutation p.Tyr2164Cys(p.Y2164C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83542224:83542224(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9221G>A
AA Mutation p.Gly3074Asp(p.G3074D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538530:83538530(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140580494
CDS Mutation c.5527G>A
AA Mutation p.Asp1843Asn(p.D1843N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540496:83540496(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7493G>A
AA Mutation p.Ser2498Asn(p.S2498N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541760:83541760(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8757A>T
AA Mutation p.Glu2919Asp(p.E2919D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83539211:83539211(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6208A>G
AA Mutation p.Lys2070Glu(p.K2070E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521119:83521119(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2813C>A
AA Mutation p.Ser938Tyr(p.S938Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521988:83521988(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772576325
CDS Mutation c.3682G>A
AA Mutation p.Ala1228Thr(p.A1228T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83490256:83490256(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.229G>T
AA Mutation p.Asp77Tyr(p.D77Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83521814:83521814(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3508A>G
AA Mutation p.Thr1170Ala(p.T1170A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540429:83540429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7426G>A
AA Mutation p.Ala2476Thr(p.A2476T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83541242:83541242(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8239A>G
AA Mutation p.Thr2747Ala(p.T2747A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265077
Start 83553522:83553522(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9652C>T
AA Mutation p.Arg3218Cys(p.R3218C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83548028:83548028(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9437T>G
AA Mutation p.Phe3146Cys(p.F3146C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538014:83538014(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5011T>G
AA Mutation p.Leu1671Val(p.L1671V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83490380:83490380(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776655704
CDS Mutation c.353T>C
AA Mutation p.Val118Ala(p.V118A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83519599:83519599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1293G>T
AA Mutation p.Lys431Asn(p.K431N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83537763:83537763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4760T>C
AA Mutation p.Val1587Ala(p.V1587A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538108:83538108(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5105C>T
AA Mutation p.Pro1702Leu(p.P1702L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538320:83538320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5317T>G
AA Mutation p.Phe1773Val(p.F1773V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538582:83538582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5579T>G
AA Mutation p.Ile1860Ser(p.I1860S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83538990:83538990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5987C>A
AA Mutation p.Thr1996Asn(p.T1996N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540009:83540009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7006T>G
AA Mutation p.Leu2336Val(p.L2336V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83540184:83540184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7181C>T
AA Mutation p.Thr2394Ile(p.T2394I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000265077
Start 83580331:83580331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10088C>A
AA Mutation p.Ser3363Tyr(p.S3363Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83522224:83522224(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768841073
CDS Mutation c.3918G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83490120:83490120(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771456960
CDS Mutation c.93G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83520400:83520400(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2094T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83521435:83521435(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3129G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83483584:83483584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.66T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83520466:83520466(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2160C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83541991:83541991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8988A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000265077
Start 83521006:83521006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2700T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence stop_gained
Transcription ID ENST00000265077
Start 83538356:83538356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5353G>T
AA Mutation p.Glu1785Ter(p.E1785*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence stop_gained
Transcription ID ENST00000265077
Start 83538734:83538734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5731C>T
AA Mutation p.Arg1911Ter(p.R1911*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence stop_gained
Transcription ID ENST00000265077
Start 83537051:83537051(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4048G>T
AA Mutation p.Glu1350Ter(p.E1350*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript