Colon Cancer: Gene >> PIAS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145856663:145856663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368T>C
AA Mutation	p.Val123Ala(p.V123A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145850489:145850489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546T>A
AA Mutation	p.Tyr516Asn(p.Y516N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145856604:145856604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Trp(p.R143W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145849558:145849558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1775G>A
AA Mutation	p.Arg592His(p.R592H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145851113:145851113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186G>A
AA Mutation	p.Glu396Lys(p.E396K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145853848:145853848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>A
AA Mutation	p.Ala317Thr(p.A317T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145856726:145856726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782639620
CDS Mutation	c.305C>T
AA Mutation	p.Ala102Val(p.A102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393045
Start	145849471:145849471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862G>A
AA Mutation	p.Arg621Gln(p.R621Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393045
Start	145850529:145850529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393045
Start	145856593:145856593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393045
Start	145855741:145855741(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.664delC
AA Mutation	p.Leu222CysfsTer56(p.L222Cfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000393045
Start	145856844:145856844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Ter(p.R63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PIAS3

No Mutation Annotation!