Colon Cancer: Gene >> PSRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409138
Start	109280429:109280429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055C>A
AA Mutation	p.Pro352His(p.P352H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409138
Start	109281882:109281882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754495062
CDS Mutation	c.256G>A
AA Mutation	p.Ala86Thr(p.A86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409138
Start	109281704:109281704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148605172
CDS Mutation	c.434C>T
AA Mutation	p.Thr145Met(p.T145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409138
Start	109281945:109281945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193A>T
AA Mutation	p.Ser65Cys(p.S65C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409138
Start	109281798:109281798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141272790
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Trp(p.R114W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000409138
Start	109282011:109282011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>T
AA Mutation	p.Arg43Ter(p.R43*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PSRC1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000409138
Start	109281765:109281765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773919831
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Ter(p.R125*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript