Colon Cancer: Gene >> PCSK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101432048:101432048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778026701
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Gln(p.R152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101398531:101398531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869A>C
AA Mutation	p.Lys290Thr(p.K290T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101431442:101431442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373433666
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Cys(p.R179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101322550:101322550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2435A>G
AA Mutation	p.Glu812Gly(p.E812G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101370422:101370422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367969161
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545His(p.R545H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101318328:101318328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2560A>G
AA Mutation	p.Thr854Ala(p.T854A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101370437:101370437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1619A>G
AA Mutation	p.Glu540Gly(p.E540G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101331954:101331954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531121474
CDS Mutation	c.1936C>T
AA Mutation	p.Arg646Cys(p.R646C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101318377:101318377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2511C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101307319:101307319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772337520
CDS Mutation	c.2706C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101322564:101322564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558140987
CDS Mutation	c.2421C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101398446:101398446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199625817
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101370472:101370472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1584C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101322585:101322585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2400C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101389517:101389517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PCSK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101389542:101389542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372460647
CDS Mutation	c.1232G>A
AA Mutation	p.Arg411His(p.R411H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611716
Start	101325041:101325041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2186G>A
AA Mutation	p.Cys729Tyr(p.C729Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101398503:101398503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762240584
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611716
Start	101393398:101393398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756842286
CDS Mutation	c.1023C>T
Mutation Classification	Silent
Feature Type	Transcript