Colon Cancer: Gene >> THBS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80080043:80080043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2650T>C
AA Mutation	p.Phe884Leu(p.F884L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80068056:80068056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278C>G
AA Mutation	p.Asn426Lys(p.N426K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80080026:80080026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2633A>C
AA Mutation	p.Lys878Thr(p.K878T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80070384:80070384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426C>T
AA Mutation	p.Pro476Ser(p.P476S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80076923:80076923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1961C>T
AA Mutation	p.Thr654Ile(p.T654I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80077037:80077037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2075A>G
AA Mutation	p.Glu692Gly(p.E692G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80065448:80065448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145442755
CDS Mutation	c.1165G>A
AA Mutation	p.Val389Ile(p.V389I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80083132:80083132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2877C>A
AA Mutation	p.Phe959Leu(p.F959L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80040120:80040120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367779999
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80079090:80079090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752904360
CDS Mutation	c.2343C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80083132:80083132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2877C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80072306:80072306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1749A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80072303:80072303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80059809:80059809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80059481:80059481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759297357
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000350881
Start	80065433:80065433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763926346
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Ter(p.R384*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> THBS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80040268:80040268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200373343
CDS Mutation	c.280C>T
AA Mutation	p.Arg94Cys(p.R94C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80070384:80070384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426C>T
AA Mutation	p.Pro476Ser(p.P476S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript