Colon Cancer: Gene >> PROS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93893024:93893024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780863931
CDS Mutation	c.1064G>A
AA Mutation	p.Arg355His(p.R355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93905898:93905898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Asp163Asn(p.D163N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93910637:93910637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>A
AA Mutation	p.Leu110Ile(p.L110I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93910697:93910697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765935815
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Cys(p.R90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93886376:93886376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>A
AA Mutation	p.Ala428Glu(p.A428E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93927312:93927312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172T>G
AA Mutation	p.Cys58Gly(p.C58G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93877106:93877106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1730T>G
AA Mutation	p.Phe577Cys(p.F577C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93892989:93892989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.His367Tyr(p.H367Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93905891:93905891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494C>T
AA Mutation	p.Ser165Leu(p.S165L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93927362:93927362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394236
Start	93874401:93874401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1875T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394236
Start	93927397:93927397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394236
Start	93898550:93898550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394236
Start	93927271:93927271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000394236
Start	93893068:93893068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020C>A
AA Mutation	p.Tyr340Ter(p.Y340*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000394236
Start	93900921:93900921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>T
AA Mutation	p.Glu204Ter(p.E204*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PROS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93900812:93900812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719C>A
AA Mutation	p.Ser240Tyr(p.S240Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394236
Start	93900804:93900804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>T
AA Mutation	p.Asp243Tyr(p.D243Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93905793:93905793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592G>T
AA Mutation	p.Asp198Tyr(p.D198Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394236
Start	93906134:93906134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356A>G
AA Mutation	p.Asp119Gly(p.D119G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394236
Start	93898523:93898523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774T>C
Mutation Classification	Silent
Feature Type	Transcript