Colon Cancer: Gene >> CAPRIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34090246:34090246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762757969
CDS Mutation	c.1361C>G
AA Mutation	p.Ala454Gly(p.A454G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34086151:34086151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054C>G
AA Mutation	p.Pro352Ala(p.P352A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34076362:34076362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Trp(p.R165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34090249:34090249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364C>T
AA Mutation	p.Thr455Ile(p.T455I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34076459:34076459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753405082
CDS Mutation	c.590G>A
AA Mutation	p.Arg197Gln(p.R197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34096596:34096596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1823G>A
AA Mutation	p.Arg608His(p.R608H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34079729:34079729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790T>C
AA Mutation	p.Ser264Pro(p.S264P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34086088:34086088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.991C>A
AA Mutation	p.Pro331Thr(p.P331T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000341394
Start	34097294:34097294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1999C>T
AA Mutation	p.Arg667Trp(p.R667W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341394
Start	34052637:34052637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341394
Start	34083043:34083043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CAPRIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34079691:34079691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201905401
CDS Mutation	c.752A>G
AA Mutation	p.Asn251Ser(p.N251S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34082976:34082976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341394
Start	34091994:34091994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1643G>T
AA Mutation	p.Ser548Ile(p.S548I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341394
Start	34099361:34099361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124G>T
Mutation Classification	Silent
Feature Type	Transcript