Colon Cancer: Gene >> PRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90981660:90981660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573547983
CDS Mutation	c.511C>T
AA Mutation	p.Arg171Cys(p.R171C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90974152:90974152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369605877
CDS Mutation	c.1445C>T
AA Mutation	p.Pro482Leu(p.P482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90974191:90974191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141668295
CDS Mutation	c.1406G>A
AA Mutation	p.Arg469Gln(p.R469Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90984743:90984743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
AA Mutation	p.Pro32Ser(p.P32S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394249
Start	90967158:90967158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394249
Start	90970461:90970461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1515C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394249
Start	90981652:90981652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394249
Start	90984024:90984024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394249
Start	90970509:90970509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773584087
CDS Mutation	c.1467C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394249
Start	90979182:90979182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755639807
CDS Mutation	c.1083C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90981650:90981650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521T>G
AA Mutation	p.Phe174Cys(p.F174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90981852:90981852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Glu133Lys(p.E133K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394249
Start	90979162:90979162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103T>G
AA Mutation	p.Phe368Cys(p.F368C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000394249
Start	90970427:90970427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768808438
CDS Mutation	c.1549C>T
AA Mutation	p.Arg517Ter(p.R517*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript