Colon Cancer: Gene >> PIAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68086682:68086682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759607395
CDS Mutation	c.401C>T
AA Mutation	p.Pro134Leu(p.P134L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68175711:68175711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244C>T
AA Mutation	p.Pro415Leu(p.P415L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68086715:68086715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434A>T
AA Mutation	p.Asp145Val(p.D145V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68176608:68176608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1435A>G
AA Mutation	p.Arg479Gly(p.R479G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68176507:68176507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139426789
CDS Mutation	c.1334C>T
AA Mutation	p.Ala445Val(p.A445V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68173763:68173763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771743634
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347Gln(p.R347Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68176539:68176539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366A>G
AA Mutation	p.Lys456Glu(p.K456E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68175714:68175714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1247T>G
AA Mutation	p.Met416Arg(p.M416R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68153597:68153597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>T
AA Mutation	p.Ser279Phe(p.S279F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68086360:68086360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>A
AA Mutation	p.Gly27Arg(p.G27R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68173797:68173797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376194188
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68086683:68086683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756448930
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68173746:68173746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1023G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000249636
Start	68176584:68176584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411G>T
AA Mutation	p.Glu471Ter(p.E471*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000249636
Start	68086595:68086595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>A
AA Mutation	p.Ser105Ter(p.S105*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PIAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68086379:68086379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68176644:68176644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471A>C
AA Mutation	p.Asn491His(p.N491H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68176629:68176629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456C>T
AA Mutation	p.Pro486Ser(p.P486S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68181258:68181258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1528A>C
AA Mutation	p.Ser510Arg(p.S510R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript