Colon Cancer: Gene >> CCAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68753863:68753863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130A>G
AA Mutation	p.Asp377Gly(p.D377G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68753881:68753881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779871042
CDS Mutation	c.1148G>A
AA Mutation	p.Arg383His(p.R383H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68749547:68749547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748256307
CDS Mutation	c.980G>A
AA Mutation	p.Arg327His(p.R327H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68765931:68765931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150G>A
AA Mutation	p.Arg717Gln(p.R717Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68754768:68754768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399C>G
AA Mutation	p.Leu467Val(p.L467V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68742448:68742448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>G
AA Mutation	p.Pro133Ala(p.P133A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68755482:68755482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571C>A
AA Mutation	p.Ala524Asp(p.A524D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265872
Start	68756327:68756327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265872
Start	68754792:68754792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265872
Start	68765944:68765944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752569768
CDS Mutation	c.2163T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265872
Start	68747178:68747178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.541delC
AA Mutation	p.Gln181LysfsTer2(p.Q181Kfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265872
Start	68771347:68771347(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2445delA
AA Mutation	p.Glu816LysfsTer75(p.E816Kfs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265872
Start	68765992:68765992(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2215delA
AA Mutation	p.Ser739ValfsTer11(p.S739Vfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000265872
Start	68755370:68755370(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1463delT
AA Mutation	p.Leu488Ter(p.L488*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000265872
Start	68749600:68749600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Ter(p.R345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000265872
Start	68749540:68749540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>T
AA Mutation	p.Glu325Ter(p.E325*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265872
Start	68740637:68740638(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.304dupC
AA Mutation	p.Gln102ProfsTer17(p.Q102Pfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265872
Start	68749262:68749262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748201128
CDS Mutation	c.953G>A
AA Mutation	p.Arg318Gln(p.R318Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript