Colon Cancer: Gene >> PRRT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813835:29813835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781G>T
AA Mutation	p.Gly261Cys(p.G261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813324:29813324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>A
AA Mutation	p.Ser90Arg(p.S90R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813325:29813325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>A
AA Mutation	p.Pro91Thr(p.P91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813439:29813439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29814445:29814445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992C>T
AA Mutation	p.Ser331Phe(p.S331F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813788:29813788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754897123
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813211:29813211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157A>C
AA Mutation	p.Asn53His(p.N53H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358758
Start	29813198:29813198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358758
Start	29813825:29813825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.776delG
AA Mutation	p.Gly259ValfsTer54(p.G259Vfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358758
Start	29813677:29813677(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.629delC
AA Mutation	p.Pro210GlnfsTer19(p.P210Qfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358758
Start	29813691:29813691(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769519069
CDS Mutation	c.640delG
AA Mutation	p.Ala214ProfsTer15(p.A214Pfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRRT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813087:29813087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33G>T
AA Mutation	p.Met11Ile(p.M11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358758
Start	29813271:29813271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>A
AA Mutation	p.Glu73Lys(p.E73K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358758
Start	29813756:29813756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript