Colon Cancer: Gene >> ST14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130198968:130198968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749228401
CDS Mutation	c.1706A>G
AA Mutation	p.Lys569Arg(p.K569R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278742
Start	130188655:130188655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>T
AA Mutation	p.Ala123Ser(p.A123S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130196418:130196418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1193C>T
AA Mutation	p.Pro398Leu(p.P398L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130208490:130208490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760328016
CDS Mutation	c.2075G>A
AA Mutation	p.Arg692His(p.R692H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130198568:130198568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1631G>A
AA Mutation	p.Cys544Tyr(p.C544Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278742
Start	130188655:130188655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>A
AA Mutation	p.Ala123Thr(p.A123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130196405:130196405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180G>A
AA Mutation	p.Ala394Thr(p.A394T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130194264:130194264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.991T>C
AA Mutation	p.Phe331Leu(p.F331L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130208639:130208639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224G>A
AA Mutation	p.Gly742Ser(p.G742S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278742
Start	130208638:130208638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2223C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278742
Start	130199044:130199044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768234714
CDS Mutation	c.1782C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278742
Start	130198405:130198405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367833176
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278742
Start	130208617:130208617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2202C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278742
Start	130189847:130189847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774428715
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000278742
Start	130188270:130188270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238C>T
AA Mutation	p.Gln80Ter(p.Q80*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ST14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278742
Start	130208466:130208466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2051G>A
AA Mutation	p.Arg684His(p.R684H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000278742
Start	130199950:130199950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript