Colon Cancer: Gene >> SERTAD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313349
Start	64636343:64636343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Glu177Lys(p.E177K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313349
Start	64636277:64636277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760388077
CDS Mutation	c.595A>G
AA Mutation	p.Thr199Ala(p.T199A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313349
Start	64636517:64636517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Asp119Asn(p.D119N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313349
Start	64636825:64636825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>T
AA Mutation	p.Gly16Val(p.G16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313349
Start	64636296:64636296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759971558
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313349
Start	64636728:64636728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313349
Start	64636647:64636647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313349
Start	64636539:64636539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779794166
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000313349
Start	64636763:64636764(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.108_109insTAGCTGT
AA Mutation	p.Arg37Ter(p.R37*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SERTAD2

No Mutation Annotation!