Colon Cancer: Gene >> RPS6KA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26572253:26572253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1907T>C
AA Mutation	p.Leu636Pro(p.L636P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26555587:26555587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878T>C
AA Mutation	p.Leu293Ser(p.L293S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26571603:26571603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768513793
CDS Mutation	c.1745C>T
AA Mutation	p.Ala582Val(p.A582V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26546876:26546876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778579909
CDS Mutation	c.118G>A
AA Mutation	p.Val40Ile(p.V40I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26536962:26536962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201278235
CDS Mutation	c.101C>T
AA Mutation	p.Pro34Leu(p.P34L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26561602:26561602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763102864
CDS Mutation	c.1529G>A
AA Mutation	p.Arg510Gln(p.R510Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26557005:26557005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989A>G
AA Mutation	p.Tyr330Cys(p.Y330C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26554662:26554662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680A>G
AA Mutation	p.Glu227Gly(p.E227G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26574103:26574103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767456589
CDS Mutation	c.2110G>A
AA Mutation	p.Ala704Thr(p.A704T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26558902:26558902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779751417
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Cys(p.R394C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26571564:26571564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706G>A
AA Mutation	p.Gly569Glu(p.G569E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374168
Start	26561510:26561510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374168
Start	26554711:26554711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760171028
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374168
Start	26571881:26571881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552205045
CDS Mutation	c.1785C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374168
Start	26555192:26555192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374168
Start	26573264:26573264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988G>A
AA Mutation	p.Arg663His(p.R663H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374168
Start	26558892:26558892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375770745
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript