Colon Cancer: Gene >> PGR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101051545:101051545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2236G>T
AA Mutation	p.Asp746Tyr(p.D746Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101062502:101062502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2157T>A
AA Mutation	p.Asn719Lys(p.N719K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101051543:101051543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199796213
CDS Mutation	c.2238C>A
AA Mutation	p.Asp746Glu(p.D746E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101051476:101051476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2305A>C
AA Mutation	p.Lys769Gln(p.K769Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101127954:101127954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>A
AA Mutation	p.Ala373Thr(p.A373T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101051562:101051562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149186732
CDS Mutation	c.2219G>A
AA Mutation	p.Arg740Gln(p.R740Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128746:101128746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Gly109Arg(p.G109R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128011:101128011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060G>A
AA Mutation	p.Ala354Thr(p.A354T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101062656:101062656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2003C>T
AA Mutation	p.Ala668Val(p.A668V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128610:101128610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461C>T
AA Mutation	p.Ala154Val(p.A154V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101042084:101042084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2507G>A
AA Mutation	p.Arg836Gln(p.R836Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101062675:101062675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150584881
CDS Mutation	c.1984G>A
AA Mutation	p.Val662Ile(p.V662I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101062662:101062662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997G>A
AA Mutation	p.Ser666Asn(p.S666N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101127811:101127811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128048:101128048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762789408
CDS Mutation	c.1023G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101041984:101041984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2607T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128960:101128960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752920291
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000325455
Start	101051563:101051563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218C>T
AA Mutation	p.Arg740Ter(p.R740*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000325455
Start	101042007:101042007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584G>T
AA Mutation	p.Gly862Ter(p.G862*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000325455
Start	101049968:101049968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2449G>T
AA Mutation	p.Glu817Ter(p.E817*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000325455
Start	101062445:101062445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PGR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101126141:101126141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1655G>A
AA Mutation	p.Ser552Asn(p.S552N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000325455
Start	101051563:101051563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218C>T
AA Mutation	p.Arg740Ter(p.R740*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000325455
Start	101062555:101062555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2104G>T
AA Mutation	p.Gly702Ter(p.G702*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript