Colon Cancer: Gene >> PRL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22290214:22290214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Thr151Ile(p.T151I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22290194:22290194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749978269
CDS Mutation	c.472A>G
AA Mutation	p.Met158Val(p.M158V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22287511:22287511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761807407
CDS Mutation	c.575G>A
AA Mutation	p.Arg192His(p.R192H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22290275:22290275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764728645
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22294489:22294489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124A>G
AA Mutation	p.Thr42Ala(p.T42A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22290197:22290197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469G>A
AA Mutation	p.Gly157Ser(p.G157S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22294450:22294450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163C>T
AA Mutation	p.His55Tyr(p.H55Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306482
Start	22294466:22294466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375151169
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306482
Start	22294547:22294547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306482
Start	22287552:22287552(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.534delG
AA Mutation	p.Trp178CysfsTer40(p.W178Cfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000306482
Start	22290317:22290317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6238
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Ter(p.R117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000306482
Start	22292599:22292600(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.250_251insGCTATT
AA Mutation	p.Asn84delinsSerTyrTyr(p.N84delinsSYY)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PRL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22290347:22290347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>A
AA Mutation	p.Asp107Asn(p.D107N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22294480:22294480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133G>T
AA Mutation	p.Asp45Tyr(p.D45Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22287425:22287425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661A>C
AA Mutation	p.Ile221Leu(p.I221L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306482
Start	22292639:22292639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201458155
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306482
Start	22290333:22290333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333G>C
Mutation Classification	Silent
Feature Type	Transcript