Colon Cancer: Gene >> RNF43

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358070:58358070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706C>A
AA Mutation	p.Pro569His(p.P569H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58362584:58362584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775028128
CDS Mutation	c.647C>T
AA Mutation	p.Ser216Leu(p.S216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58357522:58357522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747371137
CDS Mutation	c.2254G>A
AA Mutation	p.Ala752Thr(p.A752T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358466:58358466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140873038
CDS Mutation	c.1310G>A
AA Mutation	p.Arg437Gln(p.R437Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58363558:58363558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418G>A
AA Mutation	p.Asp140Asn(p.D140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58360244:58360244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857G>A
AA Mutation	p.Arg286Gln(p.R286Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358116:58358116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660C>G
AA Mutation	p.Arg554Gly(p.R554G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58360224:58360224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.877G>A
AA Mutation	p.Glu293Lys(p.E293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000407977
Start	58363600:58363600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>A
AA Mutation	p.Ala126Thr(p.A126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358164:58358164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1612C>T
AA Mutation	p.Pro538Ser(p.P538S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358292:58358292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763525805
CDS Mutation	c.1484C>A
AA Mutation	p.Ser495Tyr(p.S495Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58415330:58415330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248T>C
AA Mutation	p.Met83Thr(p.M83T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58357974:58357974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1802C>A
AA Mutation	p.Ser601Tyr(p.S601Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58415379:58415379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Gly67Cys(p.G67C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58357686:58357686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562828978
CDS Mutation	c.2090A>G
AA Mutation	p.His697Arg(p.H697R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58370937:58370937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>A
AA Mutation	p.Arg117Ser(p.R117S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58415465:58415465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113C>G
AA Mutation	p.Ser38Cys(p.S38C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58360845:58360845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201914846
CDS Mutation	c.787G>A
AA Mutation	p.Gly263Arg(p.G263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407977
Start	58363284:58363284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407977
Start	58358789:58358789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58357800:58357800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781215815
CDS Mutation	c.1976delG
AA Mutation	p.Gly659ValfsTer41(p.G659Vfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58370937:58370937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.349delC
AA Mutation	p.Arg117AlafsTer41(p.R117Afs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58363282:58363282(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.575delC
AA Mutation	p.Pro192ArgfsTer11(p.P192Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58357891:58357891(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1885delG
AA Mutation	p.Ala629ProfsTer71(p.A629Pfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58370936:58370936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.350delG
AA Mutation	p.Arg117ProfsTer41(p.R117Pfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58360218:58360218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.883delC
AA Mutation	p.His295IlefsTer124(p.H295Ifs*124)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58362632:58362632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Trp200Ter(p.W200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58363543:58363543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Ter(p.R145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58358500:58358500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276C>T
AA Mutation	p.Gln426Ter(p.Q426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58370931:58370932(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.354dupC
AA Mutation	p.Cys119LeufsTer6(p.C119Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58415482:58415483(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.95dupT
AA Mutation	p.Ala33GlyfsTer7(p.A33Gfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58358454:58358455(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1321_1322insA
AA Mutation	p.Pro441HisfsTer2(p.P441Hfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000407977
Start	58415325:58415325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.252+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RNF43

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58415333:58415333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245T>C
AA Mutation	p.Leu82Ser(p.L82S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58415451:58415451(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.127delG
AA Mutation	p.Glu43AsnfsTer8(p.E43Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58415431:58415444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.134_147delAAGCTATTATCAGA
AA Mutation	p.Lys45SerfsTer25(p.K45Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58357551:58357552(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2224dupG
AA Mutation	p.Glu742GlyfsTer5(p.E742Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript