Colon Cancer: Gene >> PSG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43071720:43071720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749542888
CDS Mutation	c.944C>T
AA Mutation	p.Ser315Leu(p.S315L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43071909:43071909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1135795
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43081094:43081094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217A>G
AA Mutation	p.Arg73Gly(p.R73G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43081180:43081180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131A>C
AA Mutation	p.Lys44Thr(p.K44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43066579:43066579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986T>G
AA Mutation	p.Leu329Arg(p.L329R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43081136:43081136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175C>T
AA Mutation	p.Pro59Ser(p.P59S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406487
Start	43080963:43080963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762496878
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406487
Start	43081056:43081056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148293206
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406487
Start	43071905:43071905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406487
Start	43075619:43075620(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.443dupA
AA Mutation	p.Pro149AlafsTer22(p.P149Afs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PSG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406487
Start	43075384:43075384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529547477
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406487
Start	43071719:43071719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1142255
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript