Colon Cancer: Gene >> PRLR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35065115:35065115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781305716
CDS Mutation	c.1843G>A
AA Mutation	p.Ala615Thr(p.A615T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35068800:35068800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764C>T
AA Mutation	p.Ala255Val(p.A255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35066098:35066098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375251112
CDS Mutation	c.860G>A
AA Mutation	p.Gly287Asp(p.G287D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35065949:35065949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>C
AA Mutation	p.Gly337Arg(p.G337R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35065213:35065213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1745C>T
AA Mutation	p.Ser582Leu(p.S582L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35070237:35070237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572T>G
AA Mutation	p.Phe191Cys(p.F191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35068230:35068230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Ala281Thr(p.A281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35065411:35065411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Asn516Ser(p.N516S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35068865:35068865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140386226
CDS Mutation	c.699T>A
AA Mutation	p.Asn233Lys(p.N233K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618457
Start	35089584:35089584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775568148
CDS Mutation	c.37C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618457
Start	35065617:35065618(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1340_1341insT
AA Mutation	p.Ala448GlyfsTer6(p.A448Gfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618457
Start	35065619:35065620(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1338_1339insT
AA Mutation	p.Pro447SerfsTer7(p.P447Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000618457
Start	35070123:35070123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRLR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35066053:35066053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905C>A
AA Mutation	p.Pro302His(p.P302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35068852:35068852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712T>C
AA Mutation	p.Trp238Arg(p.W238R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618457
Start	35068230:35068230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>C
AA Mutation	p.Ala281Pro(p.A281P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000618457
Start	35068284:35068284(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.787delA
AA Mutation	p.Met263TrpfsTer2(p.M263Wfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000618457
Start	35068286:35068286(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.786-1delG
Mutation Classification	Splice_Site
Feature Type	Transcript