Colon Cancer: Gene >> TMPRSS15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18372264:18372264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593T>C
AA Mutation	p.Ile198Thr(p.I198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18383665:18383665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458T>C
AA Mutation	p.Val153Ala(p.V153A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18313035:18313035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375777008
CDS Mutation	c.2075G>A
AA Mutation	p.Arg692Gln(p.R692Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18343974:18343974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258C>T
AA Mutation	p.Pro420Ser(p.P420S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18326530:18326530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1823C>A
AA Mutation	p.Thr608Asn(p.T608N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000284885
Start	18294605:18294605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309A>C
AA Mutation	p.Lys770Thr(p.K770T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18403600:18403600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774868000
CDS Mutation	c.23C>A
AA Mutation	p.Ser8Tyr(p.S8Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18275324:18275324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2777A>G
AA Mutation	p.Asn926Ser(p.N926S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18397895:18397895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328A>G
AA Mutation	p.Arg110Gly(p.R110G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18383674:18383674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449G>A
AA Mutation	p.Ser150Asn(p.S150N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18326515:18326515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1838C>T
AA Mutation	p.Thr613Ile(p.T613I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18332150:18332150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588C>A
AA Mutation	p.Leu530Met(p.L530M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18269995:18269995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146494364
CDS Mutation	c.3034G>A
AA Mutation	p.Glu1012Lys(p.E1012K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18278978:18278978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778496939
CDS Mutation	c.2750C>T
AA Mutation	p.Thr917Met(p.T917M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18403580:18403580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43A>G
AA Mutation	p.Ser15Gly(p.S15G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18397935:18397935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374412563
CDS Mutation	c.288C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18275269:18275269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2832G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18398241:18398241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18329218:18329218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18269996:18269996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3033C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18372287:18372287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18313055:18313055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765120268
CDS Mutation	c.2055G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18294314:18294314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369366818
CDS Mutation	c.2442C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284885
Start	18294431:18294431(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749950017
CDS Mutation	c.2325delA
AA Mutation	p.Lys775AsnfsTer58(p.K775Nfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284885
Start	18341526:18341526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1451delA
AA Mutation	p.Asn484ThrfsTer4(p.N484Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000284885
Start	18403481:18403481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Ter(p.R48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000284885
Start	18294299:18294299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2457G>A
AA Mutation	p.Trp819Ter(p.W819*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284885
Start	18294430:18294431(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2325dupA
AA Mutation	p.Leu776ThrfsTer15(p.L776Tfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TMPRSS15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18297779:18297779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2216T>C
AA Mutation	p.Val739Ala(p.V739A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18294286:18294286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2470G>A
AA Mutation	p.Ala824Thr(p.A824T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18326554:18326554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799G>T
AA Mutation	p.Gly600Val(p.G600V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18329217:18329217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732G>A
AA Mutation	p.Asp578Asn(p.D578N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18397914:18397914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309G>T
AA Mutation	p.Lys103Asn(p.K103N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284885
Start	18403600:18403600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774868000
CDS Mutation	c.23C>A
AA Mutation	p.Ser8Tyr(p.S8Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284885
Start	18344008:18344008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000284885
Start	18341452:18341452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1525G>T
AA Mutation	p.Glu509Ter(p.E509*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript