Colon Cancer: Gene >> STAC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57246833:57246833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Trp(p.R192W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57244574:57244574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769C>T
AA Mutation	p.Arg257Trp(p.R257W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57249261:57249261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114G>T
AA Mutation	p.Lys38Asn(p.K38N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57243859:57243859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048G>A
AA Mutation	p.Gly350Ser(p.G350S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57246848:57246848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559A>G
AA Mutation	p.Met187Val(p.M187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57243885:57243885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753014378
CDS Mutation	c.1022C>T
AA Mutation	p.Ala341Val(p.A341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332782
Start	57249159:57249159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143709026
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332782
Start	57244136:57244136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STAC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57246811:57246811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596A>C
AA Mutation	p.Lys199Thr(p.K199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332782
Start	57248129:57248129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502C>A
AA Mutation	p.Leu168Ile(p.L168I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript