Colon Cancer: Gene >> PIAS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4037481:4037481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>T
AA Mutation	p.Pro417Leu(p.P417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4037806:4037806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1464C>G
AA Mutation	p.Asp488Glu(p.D488E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4028752:4028752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705G>T
AA Mutation	p.Glu235Asp(p.E235D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4037834:4037834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Cys(p.R498C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4028539:4028539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611A>C
AA Mutation	p.Gln204Pro(p.Q204P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4013088:4013088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Cys(p.R65C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4013018:4013018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>T
AA Mutation	p.Arg41Ser(p.R41S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4013343:4013343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765784737
CDS Mutation	c.448G>A
AA Mutation	p.Glu150Lys(p.E150K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4033110:4033110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>T
AA Mutation	p.Lys306Asn(p.K306N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4033451:4033451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013G>A
AA Mutation	p.Arg338Gln(p.R338Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4033531:4033531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093T>C
AA Mutation	p.Cys365Arg(p.C365R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4033435:4033435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>A
AA Mutation	p.Leu333Ile(p.L333I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262971
Start	4013128:4013128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233A>G
AA Mutation	p.His78Arg(p.H78R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262971
Start	4033440:4033440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201980537
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262971
Start	4037383:4037383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147487934
CDS Mutation	c.1152G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PIAS4

No Mutation Annotation!