Colon Cancer: Gene >> PSG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342951
Start	43185130:43185130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82T>C
AA Mutation	p.Trp28Arg(p.W28R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342951
Start	43175446:43175446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733T>C
AA Mutation	p.Tyr245His(p.Y245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342951
Start	43184794:43184794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418T>C
AA Mutation	p.Phe140Leu(p.F140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342951
Start	43175224:43175224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17406362
CDS Mutation	c.955G>A
AA Mutation	p.Glu319Lys(p.E319K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342951
Start	43175264:43175264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550647828
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342951
Start	43184957:43184957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150656410
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342951
Start	43184951:43184951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342951
Start	43175456:43175456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000342951
Start	43175458:43175459(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.720_721insTGATTGCTGAAA
AA Mutation	p.Asp240_Leu241insTer(p.D240_L241ins*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PSG5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342951
Start	43175267:43175267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912T>C
Mutation Classification	Silent
Feature Type	Transcript