Colon Cancer: Gene >> SNTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33417867:33417867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553G>A
AA Mutation	p.Val185Ile(p.V185I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33410254:33410254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754648214
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373His(p.R373H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33412702:33412702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139467962
CDS Mutation	c.782C>T
AA Mutation	p.Ala261Val(p.A261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33408526:33408526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761509610
CDS Mutation	c.1499G>A
AA Mutation	p.Arg500His(p.R500H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33410225:33410225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767361112
CDS Mutation	c.1147G>A
AA Mutation	p.Val383Met(p.V383M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33408522:33408522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33417736:33417736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33412322:33412322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33410163:33410163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144821472
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33408582:33408582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530204062
CDS Mutation	c.1443G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33412328:33412328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SNTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33408591:33408591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434C>A
AA Mutation	p.Asp478Glu(p.D478E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217381
Start	33412773:33412773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.711G>T
AA Mutation	p.Glu237Asp(p.E237D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217381
Start	33408851:33408851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275G>A
Mutation Classification	Silent
Feature Type	Transcript