Colon Cancer: Gene >> SART1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312397
Start	65966199:65966199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.962G>A
AA Mutation	p.Ser321Asn(p.S321N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000312397
Start	65978914:65978914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369415657
CDS Mutation	c.2384C>T
AA Mutation	p.Ala795Val(p.A795V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312397
Start	65965774:65965774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764597455
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Trp(p.R245W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312397
Start	65966532:65966532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139408234
CDS Mutation	c.1164C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312397
Start	65978882:65978882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375131980
CDS Mutation	c.2352C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SART1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312397
Start	65976698:65976698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770434728
CDS Mutation	c.1789G>A
AA Mutation	p.Glu597Lys(p.E597K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript