Colon Cancer: Gene >> PCSK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487199:1487199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137925566
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000300954
Start	1487603:1487603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682G>A
AA Mutation	p.Gly228Ser(p.G228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1482385:1482385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1787G>A
AA Mutation	p.Cys596Tyr(p.C596Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1481917:1481917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748842152
CDS Mutation	c.2110C>T
AA Mutation	p.Arg704Cys(p.R704C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487188:1487188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775405609
CDS Mutation	c.808G>A
AA Mutation	p.Gly270Ser(p.G270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487182:1487182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369866068
CDS Mutation	c.814G>A
AA Mutation	p.Gly272Ser(p.G272S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487615:1487615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143716976
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487227:1487227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745417815
CDS Mutation	c.769G>A
AA Mutation	p.Ala257Thr(p.A257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1490190:1490190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Ala53Thr(p.A53T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487154:1487154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775454627
CDS Mutation	c.842G>A
AA Mutation	p.Arg281His(p.R281H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1482398:1482398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1774A>G
AA Mutation	p.Thr592Ala(p.T592A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000300954
Start	1487278:1487278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718A>G
AA Mutation	p.Ile240Val(p.I240V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300954
Start	1482155:1482155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1872C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300954
Start	1487841:1487841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300954
Start	1483424:1483424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000300954
Start	1484128:1484128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PCSK4

No Mutation Annotation!