Colon Cancer: Gene >> RPS6KA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20164913:20164913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750T>G
AA Mutation	p.Phe584Val(p.F584V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20195131:20195131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs122454127
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Trp(p.R114W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379565
Start	20162965:20162965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772004070
CDS Mutation	c.1840G>A
AA Mutation	p.Gly614Ser(p.G614S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20167596:20167596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595C>T
AA Mutation	p.Ala532Val(p.A532V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20176437:20176437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996G>T
AA Mutation	p.Trp332Cys(p.W332C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20194202:20194202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379565
Start	20194240:20194240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379565
Start	20155483:20155484(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2137_2138insGAACTTGTGCT
AA Mutation	p.Asn713ArgfsTer13(p.N713Rfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20167658:20167658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1533C>A
AA Mutation	p.Phe511Leu(p.F511L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20204069:20204069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278C>A
AA Mutation	p.Ala93Asp(p.A93D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20167675:20167675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516C>A
AA Mutation	p.Leu506Ile(p.L506I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379565
Start	20209391:20209391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140T>G
AA Mutation	p.Ile47Ser(p.I47S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379565
Start	20204092:20204092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255T>A
Mutation Classification	Silent
Feature Type	Transcript