Colon Cancer: Gene >> AARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70258190:70258190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2020G>T
AA Mutation	p.Ala674Ser(p.A674S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70259068:70259068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1904G>T
AA Mutation	p.Arg635Ile(p.R635I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70262468:70262468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1549G>A
AA Mutation	p.Glu517Lys(p.E517K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70252846:70252846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2782G>A
AA Mutation	p.Asp928Asn(p.D928N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70269684:70269684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896C>T
AA Mutation	p.Ala299Val(p.A299V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70269672:70269672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369366275
CDS Mutation	c.908G>A
AA Mutation	p.Arg303Gln(p.R303Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70271802:70271802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650T>C
AA Mutation	p.Leu217Pro(p.L217P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70271910:70271910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202099051
CDS Mutation	c.542C>T
AA Mutation	p.Thr181Met(p.T181M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70265039:70265039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411G>A
AA Mutation	p.Glu471Lys(p.E471K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70271957:70271957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495A>C
AA Mutation	p.Lys165Asn(p.K165N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261772
Start	70262490:70262490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261772
Start	70254636:70254636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2385C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261772
Start	70271831:70271831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147424208
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261772
Start	70258079:70258080(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2130dupC
AA Mutation	p.Ser711LeufsTer11(p.S711Lfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70270239:70270239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773A>G
AA Mutation	p.Tyr258Cys(p.Y258C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70268339:70268339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765846298
CDS Mutation	c.1003G>A
AA Mutation	p.Ala335Thr(p.A335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261772
Start	70259008:70259008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1964T>G
AA Mutation	p.Ile655Ser(p.I655S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript