Colon Cancer: Gene >> SH2B3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341259
Start	111447539:111447539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231G>A
AA Mutation	p.Ala411Thr(p.A411T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341259
Start	111418819:111418819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674G>A
AA Mutation	p.Arg225His(p.R225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341259
Start	111448267:111448267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1693C>A
AA Mutation	p.Leu565Met(p.L565M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341259
Start	111447812:111447812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374482426
CDS Mutation	c.1393G>A
AA Mutation	p.Val465Ile(p.V465I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341259
Start	111448081:111448081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507T>A
AA Mutation	p.Ser503Thr(p.S503T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341259
Start	111418274:111418274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341259
Start	111447769:111447769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772961717
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341259
Start	111447341:111447341(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1038delG
AA Mutation	p.Leu347CysfsTer26(p.L347Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341259
Start	111448135:111448135(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1566delC
AA Mutation	p.Glu523SerfsTer25(p.E523Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SH2B3

No Mutation Annotation!