Colon Cancer: Gene >> PAK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39175365:39175365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377696830
CDS Mutation	c.1286C>T
AA Mutation	p.Ser429Leu(p.S429L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39177688:39177688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774651046
CDS Mutation	c.1499C>T
AA Mutation	p.Ser500Leu(p.S500L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39169566:39169566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13A>G
AA Mutation	p.Arg5Gly(p.R5G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39173142:39173142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>T
AA Mutation	p.Glu143Asp(p.E143D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39176617:39176617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387G>A
AA Mutation	p.Ala463Thr(p.A463T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39178560:39178560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747655225
CDS Mutation	c.1757G>A
AA Mutation	p.Arg586His(p.R586H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358301
Start	39176663:39176663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433C>T
AA Mutation	p.Thr478Met(p.T478M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39178429:39178429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39175408:39175408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141004307
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39178471:39178471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39173857:39173857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39173037:39173037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55711468
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39173034:39173034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358301
Start	39177719:39177719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749356499
CDS Mutation	c.1530C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358301
Start	39173273:39173273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.565delC
AA Mutation	p.Gln189SerfsTer180(p.Q189Sfs*180)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358301
Start	39169746:39169746(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.196delG
AA Mutation	p.Ala66ProfsTer29(p.A66Pfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000358301
Start	39176641:39176641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Ter(p.R471*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PAK4

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358301
Start	39173273:39173273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.565delC
AA Mutation	p.Gln189SerfsTer180(p.Q189Sfs*180)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript