Colon Cancer: Gene >> PPP1R12A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79796824:79796824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2419A>C
AA Mutation	p.Thr807Pro(p.T807P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79832388:79832388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591A>T
AA Mutation	p.Lys197Asn(p.K197N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79934859:79934859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79934726:79934726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79786424:79786424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2857A>G
AA Mutation	p.Thr953Ala(p.T953A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79797389:79797389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2098A>T
AA Mutation	p.Thr700Ser(p.T700S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79809922:79809922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751773876
CDS Mutation	c.1328C>T
AA Mutation	p.Thr443Met(p.T443M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261207
Start	79798536:79798536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2049A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261207
Start	79934740:79934740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261207
Start	79807262:79807262(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776166170
CDS Mutation	c.1619delA
AA Mutation	p.Asn540IlefsTer23(p.N540Ifs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R12A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261207
Start	79790482:79790482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764281068
CDS Mutation	c.2651C>T
AA Mutation	p.Thr884Met(p.T884M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261207
Start	79820827:79820827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061G>T
AA Mutation	p.Ser354Ile(p.S354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript