Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47350498:47350498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014G>A
AA Mutation	p.Ala672Thr(p.A672T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349680:47349680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196C>A
AA Mutation	p.Pro399His(p.P399H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47357152:47357152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3439A>G
AA Mutation	p.Thr1147Ala(p.T1147A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47348749:47348749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265A>G
AA Mutation	p.Ile89Val(p.I89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349148:47349148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664G>A
AA Mutation	p.Gly222Ser(p.G222S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47351093:47351093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2609A>G
AA Mutation	p.Glu870Gly(p.E870G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349257:47349257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Gln(p.R258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47351176:47351176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2692G>T
AA Mutation	p.Ala898Ser(p.A898S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47348896:47348896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Val138Ile(p.V138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349782:47349782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1298C>T
AA Mutation	p.Ser433Leu(p.S433L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349812:47349812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328G>A
AA Mutation	p.Arg443His(p.R443H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349238:47349238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>A
AA Mutation	p.Ala252Thr(p.A252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47357164:47357164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3451G>A
AA Mutation	p.Ala1151Thr(p.A1151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47350808:47350808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2324C>T
AA Mutation	p.Thr775Met(p.T775M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47357162:47357162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3449C>T
AA Mutation	p.Thr1150Ile(p.T1150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47348734:47348734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>A
AA Mutation	p.Asp84Asn(p.D84N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47348795:47348795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47350767:47350767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2283G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349072:47349072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349195:47349195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47350839:47350839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2355C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349865:47349865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349528:47349528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349096:47349096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47350761:47350761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2277C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47348877:47348877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47355505:47355505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349924:47349924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000584701
Start	47349191:47349191(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.710delG
AA Mutation	p.Gly237AlafsTer33(p.G237Afs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000584701
Start	47353324:47353324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3055-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349700:47349700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1216G>A
AA Mutation	p.Glu406Lys(p.E406K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47355480:47355480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3350A>G
AA Mutation	p.Asp1117Gly(p.D1117G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47350087:47350087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1603C>T
AA Mutation	p.Arg535Cys(p.R535C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47349117:47349117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>C
AA Mutation	p.Trp211Cys(p.W211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47350321:47350321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837C>T
AA Mutation	p.Pro613Ser(p.P613S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000584701
Start	47357156:47357156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3443C>T
AA Mutation	p.Ala1148Val(p.A1148V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47349369:47349369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47348685:47348685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47353489:47353489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47353336:47353336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3066T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000584701
Start	47350221:47350221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1737G>A
Mutation Classification	Silent
Feature Type	Transcript