Colon Cancer: Gene >> WARS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119033120:119033120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201132666
CDS Mutation	c.874C>T
AA Mutation	p.Arg292Cys(p.R292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119033239:119033239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765994519
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119076474:119076474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224A>G
AA Mutation	p.Asp75Gly(p.D75G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119033300:119033300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750645277
CDS Mutation	c.694C>A
AA Mutation	p.Pro232Thr(p.P232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119032930:119032930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064A>C
AA Mutation	p.Lys355Thr(p.K355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119033152:119033152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842C>T
AA Mutation	p.Ala281Val(p.A281V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119076381:119076381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753188889
CDS Mutation	c.317C>T
AA Mutation	p.Pro106Leu(p.P106L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119033282:119033282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>A
AA Mutation	p.Val238Ile(p.V238I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235521
Start	119032961:119032961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235521
Start	119032956:119032956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235521
Start	119076557:119076557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235521
Start	119076373:119076373(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.325delA
AA Mutation	p.Ser109AlafsTer15(p.S109Afs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WARS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119076596:119076596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102G>T
AA Mutation	p.Lys34Asn(p.K34N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235521
Start	119034120:119034120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>A
AA Mutation	p.Phe203Leu(p.F203L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript