Colon Cancer: Gene >> SESN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253063
Start	28274078:28274078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940T>A
AA Mutation	p.Cys314Ser(p.C314S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253063
Start	28272726:28272726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683C>A
AA Mutation	p.Pro228His(p.P228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000253063
Start	28274042:28274042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>A
AA Mutation	p.Asp302Asn(p.D302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253063
Start	28271794:28271794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277T>C
AA Mutation	p.Phe93Leu(p.F93L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253063
Start	28280746:28280746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253063
Start	28271825:28271825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769442139
CDS Mutation	c.308C>T
AA Mutation	p.Thr103Met(p.T103M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253063
Start	28272388:28272388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376058765
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253063
Start	28280745:28280745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763448717
CDS Mutation	c.1386G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253063
Start	28273387:28273387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117161934
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253063
Start	28274048:28274048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253063
Start	28272760:28272760(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.722delC
AA Mutation	p.Pro241GlnfsTer6(p.P241Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253063
Start	28272740:28272740(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.701delC
AA Mutation	p.Pro234LeufsTer13(p.P234Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SESN2

No Mutation Annotation!