Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAGEC1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907820:141907820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2416G>T
AA Mutation p.Ala806Ser(p.A806S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908542:141908542(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753057119
CDS Mutation c.3138A>C
AA Mutation p.Lys1046Asn(p.K1046N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141906635:141906635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1231C>A
AA Mutation p.Pro411Thr(p.P411T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908573:141908573(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141172739
CDS Mutation c.3169C>T
AA Mutation p.Arg1057Trp(p.R1057W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905460:141905460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.56C>T
AA Mutation p.Ser19Phe(p.S19F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141906006:141906006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.602C>A
AA Mutation p.Pro201His(p.P201H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907500:141907500(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2096T>C
AA Mutation p.Leu699Pro(p.L699P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907821:141907821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2417C>T
AA Mutation p.Ala806Val(p.A806V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907906:141907906(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2502C>A
AA Mutation p.Phe834Leu(p.F834L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908211:141908211(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2807C>A
AA Mutation p.Thr936Lys(p.T936K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141906992:141906992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1588C>A
AA Mutation p.Leu530Ile(p.L530I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907659:141907659(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2255C>A
AA Mutation p.Ser752Tyr(p.S752Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905491:141905491(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.87G>T
AA Mutation p.Glu29Asp(p.E29D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905846:141905846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.442C>A
AA Mutation p.Pro148Thr(p.P148T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907191:141907191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1787C>T
AA Mutation p.Pro596Leu(p.P596L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908059:141908059(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769947583
CDS Mutation c.2655G>T
AA Mutation p.Leu885Phe(p.L885F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908705:141908705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3301T>A
AA Mutation p.Ser1101Thr(p.S1101T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907021:141907021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1617G>C
AA Mutation p.Trp539Cys(p.W539C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907245:141907245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1841G>T
AA Mutation p.Ser614Ile(p.S614I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907820:141907820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2416G>A
AA Mutation p.Ala806Thr(p.A806T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905770:141905770(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.366G>T
AA Mutation p.Glu122Asp(p.E122D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907593:141907593(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2189C>A
AA Mutation p.Pro730His(p.P730H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905779:141905779(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.375G>C
AA Mutation p.Gln125His(p.Q125H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907923:141907923(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372547539
CDS Mutation c.2519C>T
AA Mutation p.Ser840Leu(p.S840L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907286:141907286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1882C>T
AA Mutation p.Pro628Ser(p.P628S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907095:141907095(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1691T>G
AA Mutation p.Phe564Cys(p.F564C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000285879
Start 141905409:141905409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5G>A
AA Mutation p.Gly2Glu(p.G2E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907320:141907320(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1916G>A
AA Mutation p.Ser639Asn(p.S639N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908289:141908289(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2885G>A
AA Mutation p.Gly962Asp(p.G962D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141906474:141906474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1070C>A
AA Mutation p.Ser357Tyr(p.S357Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907434:141907434(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2030A>G
AA Mutation p.Gln677Arg(p.Q677R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908775:141908775(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747835069
CDS Mutation c.3371C>T
AA Mutation p.Ser1124Leu(p.S1124L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908151:141908151(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776851614
CDS Mutation c.2747C>T
AA Mutation p.Ala916Val(p.A916V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141906400:141906400(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.996T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141905440:141905440(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.36G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141907855:141907855(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2451C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141905539:141905539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781697121
CDS Mutation c.135C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141905671:141905671(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138220840
CDS Mutation c.267C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141908830:141908830(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753289732
CDS Mutation c.3426G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141907039:141907039(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1635T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141908353:141908353(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371741859
CDS Mutation c.2949C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141907894:141907894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2490T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141908152:141908152(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749815753
CDS Mutation c.2748G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141907657:141907657(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2253T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000285879
Start 141907600:141907600(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2200delG
AA Mutation p.Glu734ArgfsTer11(p.E734Rfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence stop_gained
Transcription ID ENST00000285879
Start 141908738:141908738(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3334G>T
AA Mutation p.Glu1112Ter(p.E1112*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000285879
Start 141908132:141908133(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2732dupA
AA Mutation p.Val912GlyfsTer44(p.V912Gfs*44)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 48
Mutation Consequence splice_donor_variant;5_prime_UTR_variant;intron_variant
Transcription ID ENST00000285879
Start 141904801:141904828(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.-115_-104+16delCCAGGAGTCAAGGTGAGTGCACGACCTG
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> MAGEC1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905661:141905661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257C>A
AA Mutation p.Ser86Tyr(p.S86Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908699:141908699(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3295T>A
AA Mutation p.Phe1099Ile(p.F1099I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141907874:141907874(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2470A>T
AA Mutation p.Ser824Cys(p.S824C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141906694:141906694(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1290T>G
AA Mutation p.Ser430Arg(p.S430R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908104:141908104(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2700C>A
AA Mutation p.Ser900Arg(p.S900R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908573:141908573(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141172739
CDS Mutation c.3169C>T
AA Mutation p.Arg1057Trp(p.R1057W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905587:141905587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.183G>T
AA Mutation p.Glu61Asp(p.E61D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908282:141908282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2878C>T
AA Mutation p.Leu960Phe(p.L960F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141908680:141908680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3276G>T
AA Mutation p.Lys1092Asn(p.K1092N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141905704:141905704(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.300G>T
AA Mutation p.Gln100His(p.Q100H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000285879
Start 141906216:141906216(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.812C>T
AA Mutation p.Pro271Leu(p.P271L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141906493:141906493(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1089T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000285879
Start 141906388:141906388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.984T>C
Mutation Classification Silent
Feature Type Transcript