Colon Cancer: Gene >> CHST5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75530167:75530167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>T
AA Mutation	p.Ser73Leu(p.S73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75530164:75530164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221G>T
AA Mutation	p.Gly74Val(p.G74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75530282:75530282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103C>A
AA Mutation	p.Leu35Ile(p.L35I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75530045:75530045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572591635
CDS Mutation	c.340G>A
AA Mutation	p.Val114Met(p.V114M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75529924:75529924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765605385
CDS Mutation	c.461C>T
AA Mutation	p.Pro154Leu(p.P154L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75529342:75529342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748093814
CDS Mutation	c.1043C>T
AA Mutation	p.Ala348Val(p.A348V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75530041:75530041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344G>A
AA Mutation	p.Arg115His(p.R115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336257
Start	75529499:75529499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.886G>A
AA Mutation	p.Glu296Lys(p.E296K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336257
Start	75529917:75529917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHST5

No Mutation Annotation!