Colon Cancer: Gene >> GIPC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3590158:3590158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769307495
CDS Mutation	c.907G>A
AA Mutation	p.Ala303Thr(p.A303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3586842:3586842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141293401
CDS Mutation	c.440G>A
AA Mutation	p.Arg147Gln(p.R147Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3586931:3586931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>A
AA Mutation	p.Leu177Ile(p.L177I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3586585:3586585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>A
AA Mutation	p.Val106Met(p.V106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3590072:3590072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149028750
CDS Mutation	c.821C>T
AA Mutation	p.Ala274Val(p.A274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3586874:3586874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772741956
CDS Mutation	c.472G>A
AA Mutation	p.Glu158Lys(p.E158K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3585784:3585784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>A
AA Mutation	p.Ala63Thr(p.A63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322315
Start	3586636:3586636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>T
AA Mutation	p.Gly123Trp(p.G123W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322315
Start	3586867:3586867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322315
Start	3589869:3589869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322315
Start	3585753:3585753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322315
Start	3586846:3586846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GIPC3

No Mutation Annotation!