Colon Cancer: Gene >> CYP2S1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41203500:41203500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027A>C
AA Mutation	p.Ser343Arg(p.S343R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41203602:41203602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755173146
CDS Mutation	c.1129C>T
AA Mutation	p.Arg377Trp(p.R377W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41194680:41194680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202034225
CDS Mutation	c.314C>T
AA Mutation	p.Ala105Val(p.A105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41203585:41203585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112T>A
AA Mutation	p.Ile371Lys(p.I371K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41206475:41206475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759878389
CDS Mutation	c.1502C>T
AA Mutation	p.Thr501Met(p.T501M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41197841:41197841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768581980
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Trp(p.R136W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310054
Start	41198862:41198862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199534151
CDS Mutation	c.808G>A
AA Mutation	p.Asp270Asn(p.D270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310054
Start	41193435:41193435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310054
Start	41197852:41197852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2S1

No Mutation Annotation!