Colon Cancer: Gene >> SESN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95185461:95185461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557C>A
AA Mutation	p.Ser186Tyr(p.S186Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95184491:95184491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746291519
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95185367:95185367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651T>G
AA Mutation	p.Asp217Glu(p.D217E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95191475:95191475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781016923
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Trp(p.R91W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95184465:95184465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892C>A
AA Mutation	p.Leu298Ile(p.L298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95191454:95191454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Cys(p.R98C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000536441
Start	95191422:95191422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000536441
Start	95184541:95184541(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.816delT
AA Mutation	p.Gln273LysfsTer14(p.Q273Kfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000536441
Start	95185474:95185474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>T
AA Mutation	p.Glu182Ter(p.E182*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SESN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95185440:95185440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578C>T
AA Mutation	p.Ala193Val(p.A193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000536441
Start	95185398:95185398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620T>A
AA Mutation	p.Val207Asp(p.V207D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript