Colon Cancer: Gene >> PICK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356976
Start	38074869:38074869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Asp329Asn(p.D329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356976
Start	38074392:38074392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920G>A
AA Mutation	p.Arg307His(p.R307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356976
Start	38071741:38071741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199868329
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Trp(p.R185W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356976
Start	38075096:38075096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356976
Start	38073020:38073020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356976
Start	38067739:38067739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770980114
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356976
Start	38072550:38072550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142805203
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356976
Start	38065088:38065089(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.244dupA
AA Mutation	p.Thr82AsnfsTer2(p.T82Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PICK1

No Mutation Annotation!