Colon Cancer: Gene >> CCAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22605820:22605820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Arg16His(p.R16H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22619311:22619311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556131395
CDS Mutation	c.2683C>T
AA Mutation	p.Arg895Cys(p.R895C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22614981:22614981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185T>A
AA Mutation	p.Asp395Glu(p.D395E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22614225:22614225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778848959
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Trp(p.R280W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22619665:22619665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2755C>T
AA Mutation	p.Pro919Ser(p.P919S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22607011:22607011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344C>T
AA Mutation	p.Thr115Met(p.T115M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22616225:22616225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1822G>A
AA Mutation	p.Ala608Thr(p.A608T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22618651:22618651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2255A>G
AA Mutation	p.Asn752Ser(p.N752S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22606100:22606100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74C>T
AA Mutation	p.Ser25Phe(p.S25F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308511
Start	22614945:22614945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115014172
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308511
Start	22614934:22614934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22615811:22615811(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1513delC
AA Mutation	p.Leu505Ter(p.L505*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22615462:22615462(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1249delC
AA Mutation	p.Arg417GlyfsTer89(p.R417Gfs*89)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22606684:22606685(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.234dupT
AA Mutation	p.Gln79SerfsTer14(p.Q79Sfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22615836:22615836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532C>A
AA Mutation	p.Ala511Glu(p.A511E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22614941:22614941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22613035:22613035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603G>T
AA Mutation	p.Lys201Asn(p.K201N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22615811:22615811(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1513delC
AA Mutation	p.Leu505Ter(p.L505*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript