Colon Cancer: Gene >> CLASRP

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000221455
Start	45062195:45062195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Gln(p.R302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45062186:45062186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776111579
CDS Mutation	c.896C>T
AA Mutation	p.Pro299Leu(p.P299L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45070838:45070838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779406462
CDS Mutation	c.2018G>A
AA Mutation	p.Arg673Gln(p.R673Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45040264:45040264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Asp18Asn(p.D18N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45064071:45064071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45053165:45053165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367G>C
AA Mutation	p.Asp123His(p.D123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45064073:45064073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>A
AA Mutation	p.Glu323Lys(p.E323K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000221455
Start	45064070:45064070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759794192
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Cys(p.R322C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221455
Start	45056478:45056478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221455
Start	45068018:45068018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221455
Start	45052871:45052871(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.284delC
AA Mutation	p.Pro95LeufsTer81(p.P95Lfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000221455
Start	45070048:45070050(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1901_1903delGAG
AA Mutation	p.Arg634_Glu635delinsLys(p.R634_E635delinsK)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CLASRP

No Mutation Annotation!