Colon Cancer: Gene >> PSD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18867987:18867987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321T>A
AA Mutation	p.Tyr441Asn(p.Y441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18655665:18655665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2196G>T
AA Mutation	p.Lys732Asn(p.K732N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18804598:18804598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753810304
CDS Mutation	c.1834G>A
AA Mutation	p.Glu612Lys(p.E612K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440756
Start	18804874:18804874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440756
Start	18872693:18872693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440756
Start	18871793:18871793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440756
Start	18867748:18867748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143433674
CDS Mutation	c.1560C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440756
Start	18804557:18804557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1875delT
AA Mutation	p.Phe625LeufsTer6(p.F625Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440756
Start	18556275:18556275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2865delC
AA Mutation	p.Asp956ThrfsTer14(p.D956Tfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440756
Start	18632699:18632699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2327delT
AA Mutation	p.Leu776TrpfsTer44(p.L776Wfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000440756
Start	18632658:18632658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2368G>T
AA Mutation	p.Gly790Ter(p.G790*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440756
Start	18556274:18556275(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2865dupC
AA Mutation	p.Asp956ArgfsTer11(p.D956Rfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440756
Start	18801329:18801330(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1962_1963dupAG
AA Mutation	p.Val655GlufsTer3(p.V655Efs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PSD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18871881:18871881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983G>T
AA Mutation	p.Arg328Ile(p.R328I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18867780:18867780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528G>T
AA Mutation	p.Asp510Tyr(p.D510Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18871903:18871903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>T
AA Mutation	p.Asp321Tyr(p.D321Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000440756
Start	18632638:18632638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2388T>G
AA Mutation	p.Ile796Met(p.I796M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440756
Start	18535857:18535857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547134848
CDS Mutation	c.3033G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440756
Start	18575239:18575239(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2531delA
AA Mutation	p.Asn844ThrfsTer3(p.N844Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript