Colon Cancer: Gene >> THSD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397275:52397275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978T>A
AA Mutation	p.His326Gln(p.H326Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397317:52397317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936G>T
AA Mutation	p.Lys312Asn(p.K312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378577:52378577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773080927
CDS Mutation	c.1393G>A
AA Mutation	p.Glu465Lys(p.E465K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52386033:52386033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175G>C
AA Mutation	p.Cys392Ser(p.C392S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52377937:52377937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2033C>T
AA Mutation	p.Ala678Val(p.A678V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397536:52397536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717A>C
AA Mutation	p.Lys239Asn(p.K239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52397327:52397327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926A>G
AA Mutation	p.Asp309Gly(p.D309G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52377936:52377936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2034C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52397569:52397569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52377681:52377681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2289G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52378332:52378332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767346586
CDS Mutation	c.1638G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52378461:52378461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1509G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52398100:52398100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52378272:52378272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753100705
CDS Mutation	c.1698G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000258613
Start	52377783:52377783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2187C>A
AA Mutation	p.Tyr729Ter(p.Y729*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> THSD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378108:52378108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772529936
CDS Mutation	c.1862G>T
AA Mutation	p.Ser621Ile(p.S621I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258613
Start	52378379:52378379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1591C>T
AA Mutation	p.Arg531Cys(p.R531C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258613
Start	52378647:52378647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>C
Mutation Classification	Silent
Feature Type	Transcript