Colon Cancer: Gene >> RPS6KA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64361152:64361152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481G>T
AA Mutation	p.Asp161Tyr(p.D161Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334205
Start	64365302:64365302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908G>A
AA Mutation	p.Gly303Asp(p.G303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64369883:64369883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1787G>A
AA Mutation	p.Gly596Asp(p.G596D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64369885:64369885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789G>A
AA Mutation	p.Val597Ile(p.V597I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64369566:64369566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549G>A
AA Mutation	p.Val517Met(p.V517M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64370336:64370336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909G>A
AA Mutation	p.Gly637Arg(p.G637R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64368592:64368592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325T>C
AA Mutation	p.Leu442Pro(p.L442P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64365380:64365380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>A
AA Mutation	p.Gly329Asp(p.G329D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334205
Start	64370382:64370382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755881487
CDS Mutation	c.1955G>A
AA Mutation	p.Arg652Gln(p.R652Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334205
Start	64369602:64369602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585C>T
AA Mutation	p.Arg529Cys(p.R529C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334205
Start	64370344:64370344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334205
Start	64360248:64360248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334205
Start	64368137:64368137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KA4

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000334205
Start	64368131:64368131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript