Colon Cancer: Gene >> GALNS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268695
Start	88835339:88835339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779257235
CDS Mutation	c.772G>A
AA Mutation	p.Val258Ile(p.V258I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268695
Start	88814460:88814460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548G>T
AA Mutation	p.Lys516Asn(p.K516N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268695
Start	88826729:88826729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112C>T
AA Mutation	p.Thr371Ile(p.T371I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268695
Start	88814482:88814482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526C>T
AA Mutation	p.Thr509Ile(p.T509I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268695
Start	88841965:88841965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251C>T
AA Mutation	p.Ala84Val(p.A84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268695
Start	88824848:88824848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376919708
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268695
Start	88842779:88842779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373639234
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268695
Start	88835253:88835253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140299014
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268695
Start	88835244:88835244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781525725
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GALNS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268695
Start	88837748:88837748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780393705
CDS Mutation	c.440C>T
AA Mutation	p.Pro147Leu(p.P147L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript