Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EPHA3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89209988:89209988(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369150999
CDS Mutation c.282G>T
AA Mutation p.Lys94Asn(p.K94N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89413185:89413185(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1807G>A
AA Mutation p.Glu603Lys(p.E603K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89209954:89209954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.248G>A
AA Mutation p.Arg83Lys(p.R83K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89341825:89341825(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1041G>C
AA Mutation p.Trp347Cys(p.W347C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89399411:89399411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1525A>T
AA Mutation p.Ile509Phe(p.I509F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210182:89210182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.476A>G
AA Mutation p.Asp159Gly(p.D159G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89419267:89419267(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1951G>A
AA Mutation p.Ala651Thr(p.A651T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89341036:89341036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.935G>A
AA Mutation p.Arg312Gln(p.R312Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89472475:89472475(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2702T>G
AA Mutation p.Leu901Arg(p.L901R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89341779:89341779(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.995T>C
AA Mutation p.Val332Ala(p.V332A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89431319:89431319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2306G>A
AA Mutation p.Arg769His(p.R769H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89431235:89431235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2222G>A
AA Mutation p.Gly741Asp(p.G741D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89472490:89472490(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2717G>T
AA Mutation p.Ser906Ile(p.S906I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89395891:89395891(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1361C>T
AA Mutation p.Ser454Phe(p.S454F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210460:89210460(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.754G>T
AA Mutation p.Val252Leu(p.V252L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89341035:89341035(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746351940
CDS Mutation c.934C>T
AA Mutation p.Arg312Trp(p.R312W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89431160:89431160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2147C>T
AA Mutation p.Ala716Val(p.A716V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210402:89210402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.696C>A
AA Mutation p.Asn232Lys(p.N232K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89342055:89342055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1271A>G
AA Mutation p.Gln424Arg(p.Q424R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89209943:89209943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.237C>A
AA Mutation p.Asn79Lys(p.N79K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89107768:89107768(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.20T>C
AA Mutation p.Ile7Thr(p.I7T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210070:89210070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.364C>A
AA Mutation p.Leu122Met(p.L122M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210200:89210200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.494A>G
AA Mutation p.Asn165Ser(p.N165S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89210327:89210327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.621G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89340974:89340974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.873G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89399413:89399413(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1527C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89395856:89395856(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552354794
CDS Mutation c.1326G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89419305:89419305(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1989G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89341795:89341795(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201113556
CDS Mutation c.1011C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89413163:89413163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1785T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000336596
Start 89450213:89450213(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2538delC
AA Mutation p.Met847TrpfsTer10(p.M847Wfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000336596
Start 89419248:89419248(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1938delA
AA Mutation p.Glu647ArgfsTer9(p.E647Rfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000336596
Start 89341796:89341796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1012G>T
AA Mutation p.Glu338Ter(p.E338*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000336596
Start 89210477:89210477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771T>A
AA Mutation p.Cys257Ter(p.C257*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000336596
Start 89341937:89341937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1153C>T
AA Mutation p.Arg385Ter(p.R385*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000336596
Start 89341865:89341866(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1081_1082insAAGAT
AA Mutation p.Ile361LysfsTer12(p.I361Kfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> EPHA3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89399402:89399402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1516G>A
AA Mutation p.Val506Ile(p.V506I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210368:89210368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.662A>T
AA Mutation p.Gln221Leu(p.Q221L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89210369:89210369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.663G>T
AA Mutation p.Gln221His(p.Q221H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89399418:89399418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1532C>T
AA Mutation p.Ala511Val(p.A511V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000336596
Start 89209988:89209988(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369150999
CDS Mutation c.282G>T
AA Mutation p.Lys94Asn(p.K94N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89210279:89210279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.573C>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000336596
Start 89341972:89341972(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1188G>T
Mutation Classification Silent
Feature Type Transcript