Colon Cancer: Gene >> RARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231572
Start	168497286:168497286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760G>A
AA Mutation	p.Asp254Asn(p.D254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231572
Start	168519087:168519087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1880T>C
AA Mutation	p.Ile627Thr(p.I627T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231572
Start	168488614:168488614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58A>C
AA Mutation	p.Lys20Gln(p.K20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231572
Start	168500696:168500696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Leu310Phe(p.L310F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231572
Start	168500715:168500715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231572
Start	168510617:168510617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231572
Start	168506820:168506820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231572
Start	168495404:168495404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231572
Start	168493946:168493949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.422_425delTTAC
AA Mutation	p.Ile141ThrfsTer25(p.I141Tfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231572
Start	168516860:168516860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535G>T
AA Mutation	p.Arg512Leu(p.R512L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000231572
Start	168488731:168488731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749027104
CDS Mutation	c.175C>T
AA Mutation	p.Arg59Ter(p.R59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript