Colon Cancer: Gene >> PRCC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156786975:156786975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884T>A
AA Mutation	p.Ile295Asn(p.I295N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156782319:156782319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506C>A
AA Mutation	p.Thr169Asn(p.T169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156794767:156794767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282A>C
AA Mutation	p.Lys428Gln(p.K428Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156800387:156800387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403A>C
AA Mutation	p.Glu468Ala(p.E468A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156767979:156767979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775602188
CDS Mutation	c.208C>A
AA Mutation	p.Pro70Thr(p.P70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156794671:156794671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Trp(p.R396W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271526
Start	156787034:156787034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142005569
CDS Mutation	c.943G>A
AA Mutation	p.Asp315Asn(p.D315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271526
Start	156768062:156768062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271526
Start	156786718:156786718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757081137
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271526
Start	156786895:156786895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143528416
CDS Mutation	c.804T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271526
Start	156787047:156787047(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.961delC
AA Mutation	p.Glu322AsnfsTer105(p.E322Nfs*105)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271526
Start	156797312:156797312(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1362delA
AA Mutation	p.Lys454AsnfsTer18(p.K454Nfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271526
Start	156768041:156768041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.275delC
AA Mutation	p.Pro92HisfsTer5(p.P92Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRCC

No Mutation Annotation!