Colon Cancer: Gene >> RNF40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30763244:30763244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>T
AA Mutation	p.Asp87Tyr(p.D87Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766834:30766834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766821:30766821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1374G>C
AA Mutation	p.Glu458Asp(p.E458D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766212:30766212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043G>A
AA Mutation	p.Ser348Asn(p.S348N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30768508:30768508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1957A>G
AA Mutation	p.Lys653Glu(p.K653E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766263:30766263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755165767
CDS Mutation	c.1094G>A
AA Mutation	p.Arg365Gln(p.R365Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30774004:30774004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751717345
CDS Mutation	c.2896G>A
AA Mutation	p.Val966Ile(p.V966I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30772111:30772111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2750G>A
AA Mutation	p.Arg917His(p.R917H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766412:30766412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770830631
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Trp(p.R383W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30768338:30768338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1787C>G
AA Mutation	p.Ala596Gly(p.A596G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766772:30766772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146102570
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442His(p.R442H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30771884:30771884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773367988
CDS Mutation	c.2638G>A
AA Mutation	p.Val880Met(p.V880M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766442:30766442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>A
AA Mutation	p.Ala393Thr(p.A393T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30769569:30769569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777382766
CDS Mutation	c.2555G>A
AA Mutation	p.Arg852His(p.R852H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30774026:30774026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2918G>A
AA Mutation	p.Arg973Gln(p.R973Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30766798:30766798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351A>G
AA Mutation	p.Thr451Ala(p.T451A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30768439:30768439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371990879
CDS Mutation	c.1888G>A
AA Mutation	p.Ala630Thr(p.A630T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30768359:30768359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1808G>A
AA Mutation	p.Gly603Asp(p.G603D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30763271:30763271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200908487
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30765267:30765267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146962748
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30769305:30769305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2367A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30766800:30766800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200241748
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30762665:30762665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30762578:30762578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30766546:30766546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369667427
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30763169:30763169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184C>T
AA Mutation	p.Arg62Trp(p.R62W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324685
Start	30764200:30764200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759164445
CDS Mutation	c.464G>A
AA Mutation	p.Arg155Gln(p.R155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324685
Start	30763255:30763255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270A>G
Mutation Classification	Silent
Feature Type	Transcript