Colon Cancer: Gene >> PPP2R5D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	43010945:43010945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769459377
CDS Mutation	c.1619C>T
AA Mutation	p.Thr540Ile(p.T540I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	43008241:43008241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898C>A
AA Mutation	p.Leu300Ile(p.L300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	43006994:43006994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406C>T
AA Mutation	p.Leu136Phe(p.L136F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	43007999:43007999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764831855
CDS Mutation	c.791G>A
AA Mutation	p.Arg264His(p.R264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485511
Start	43008210:43008210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759229882
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485511
Start	43010985:43010985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1659T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485511
Start	43009203:43009203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777160376
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485511
Start	43006486:43006486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000485511
Start	43006583:43006583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.231delG
AA Mutation	p.Gln79ArgfsTer28(p.Q79Rfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000485511
Start	42989614:42989614(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.36delC
AA Mutation	p.Lys13ArgfsTer94(p.K13Rfs*94)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000485511
Start	43006550:43006550(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.198delC
AA Mutation	p.Thr67ArgfsTer40(p.T67Rfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPP2R5D

No Mutation Annotation!