Colon Cancer: Gene >> TRIM9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50982031:50982031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1676C>T
AA Mutation	p.Thr559Ile(p.T559I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094887:51094887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53G>A
AA Mutation	p.Arg18Gln(p.R18Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094612:51094612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>A
AA Mutation	p.Ala110Thr(p.A110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094870:51094870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70C>G
AA Mutation	p.Pro24Ala(p.P24A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094384:51094384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556G>A
AA Mutation	p.Asp186Asn(p.D186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50981812:50981812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1895C>T
AA Mutation	p.Ser632Leu(p.S632L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50982073:50982073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634C>T
AA Mutation	p.Ala545Val(p.A545V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51000730:51000730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767636523
CDS Mutation	c.1417G>A
AA Mutation	p.Asp473Asn(p.D473N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000298355
Start	51000840:51000840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307C>T
AA Mutation	p.Ala436Val(p.A436V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50981911:50981911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1796C>T
AA Mutation	p.Ala599Val(p.A599V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094494:51094494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094318:51094318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746028500
CDS Mutation	c.622C>G
AA Mutation	p.Arg208Gly(p.R208G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298355
Start	50977318:50977318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2106C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298355
Start	51094274:51094274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298355
Start	51094238:51094238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298355
Start	51000776:51000776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544784389
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298355
Start	51094667:51094667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298355
Start	51094220:51094220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298355
Start	51094138:51094138(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.802delG
AA Mutation	p.Ala268ProfsTer14(p.A268Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000298355
Start	51009187:51009187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199G>A
AA Mutation	p.Trp400Ter(p.W400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298355
Start	50979486:50979487(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1970dupA
AA Mutation	p.Asn657LysfsTer9(p.N657Kfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50981909:50981909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Cys(p.R600C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	51094288:51094288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652A>C
AA Mutation	p.Ser218Arg(p.S218R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50979467:50979467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751149890
CDS Mutation	c.1990G>A
AA Mutation	p.Asp664Asn(p.D664N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298355
Start	50979442:50979442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2015T>G
AA Mutation	p.Phe672Cys(p.F672C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript