Colon Cancer: Gene >> PPP1R10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30601999:30601999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2650G>A
AA Mutation	p.Asp884Asn(p.D884N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30608875:30608875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234G>T
AA Mutation	p.Trp78Cys(p.W78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30602173:30602173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2476G>T
AA Mutation	p.Gly826Cys(p.G826C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30605002:30605002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946G>A
AA Mutation	p.Ala316Thr(p.A316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30605947:30605947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829A>C
AA Mutation	p.Lys277Gln(p.K277Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30608808:30608808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301C>A
AA Mutation	p.Leu101Ile(p.L101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30602326:30602326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761017174
CDS Mutation	c.2323G>A
AA Mutation	p.Gly775Ser(p.G775S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30606584:30606584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.518G>A
AA Mutation	p.Arg173Gln(p.R173Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376511
Start	30602351:30602351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2298A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376511
Start	30602386:30602398(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2251_2263delCATCGTCCTCACG
AA Mutation	p.His751LysfsTer162(p.H751Kfs*162)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376511
Start	30601557:30601557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2815delC
AA Mutation	p.Leu939CysfsTer109(p.L939Cfs*109)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000376511
Start	30601969:30601969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2680C>T
AA Mutation	p.Arg894Ter(p.R894*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376511
Start	30602386:30602386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772675490
CDS Mutation	c.2263G>A
AA Mutation	p.Glu755Lys(p.E755K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376511
Start	30608869:30608869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240G>T
Mutation Classification	Silent
Feature Type	Transcript