Colon Cancer: Gene >> THBS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155197503:155197503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2459C>G
AA Mutation	p.Thr820Arg(p.T820R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155207861:155207861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>T
AA Mutation	p.Leu6Phe(p.L6F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368378
Start	155205060:155205060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543G>T
AA Mutation	p.Gln181His(p.Q181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155201472:155201472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274C>A
AA Mutation	p.Pro425His(p.P425H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155206400:155206400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86A>G
AA Mutation	p.Asp29Gly(p.D29G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155201511:155201511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235G>A
AA Mutation	p.Cys412Tyr(p.C412Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155198597:155198597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886G>T
AA Mutation	p.Gly629Val(p.G629V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155206313:155206313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173T>C
AA Mutation	p.Leu58Pro(p.L58P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368378
Start	155203086:155203086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372932762
CDS Mutation	c.808G>A
AA Mutation	p.Gly270Ser(p.G270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368378
Start	155198527:155198527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1956C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368378
Start	155200046:155200046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146879343
CDS Mutation	c.1776C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368378
Start	155197157:155197157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2556T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368378
Start	155198560:155198560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1923G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000368378
Start	155197177:155197177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748612538
CDS Mutation	c.2536C>T
AA Mutation	p.Arg846Ter(p.R846*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368378
Start	155207823:155207824(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.53dupT
AA Mutation	p.Thr19HisfsTer11(p.T19Hfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> THBS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155202013:155202013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120T>G
AA Mutation	p.Cys374Gly(p.C374G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368378
Start	155201544:155201544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751959993
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401His(p.R401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368378
Start	155201151:155201151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148689308
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript