Colon Cancer: Gene >> PROKR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68655127:68655127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>A
AA Mutation	p.Val245Met(p.V245M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68655378:68655378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>T
AA Mutation	p.Glu328Asp(p.E328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68654975:68654975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581C>T
AA Mutation	p.Ala194Val(p.A194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68646197:68646197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771784209
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Cys(p.R126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68645960:68645960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>T
AA Mutation	p.Asp47Tyr(p.D47Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68655331:68655331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201464916
CDS Mutation	c.937G>A
AA Mutation	p.Val313Met(p.V313M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68646296:68646296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769119228
CDS Mutation	c.475G>A
AA Mutation	p.Ala159Thr(p.A159T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68654974:68654974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773486402
CDS Mutation	c.580G>A
AA Mutation	p.Ala194Thr(p.A194T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68646125:68646125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200238619
CDS Mutation	c.304G>A
AA Mutation	p.Ala102Thr(p.A102T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68655442:68655442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>A
AA Mutation	p.Val350Ile(p.V350I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68655310:68655310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143892402
CDS Mutation	c.916G>A
AA Mutation	p.Val306Met(p.V306M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68655287:68655287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780773340
CDS Mutation	c.893C>T
AA Mutation	p.Ala298Val(p.A298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68646128:68646128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307A>G
AA Mutation	p.Asn103Asp(p.N103D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000303786
Start	68646119:68646119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772023504
CDS Mutation	c.298C>T
AA Mutation	p.Leu100Phe(p.L100F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68655123:68655123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68655012:68655012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68655123:68655123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68654901:68654901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753964952
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68655045:68655045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68654946:68654946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PROKR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68655309:68655309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780436849
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303786
Start	68655288:68655288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript