Colon Cancer: Gene >> IRS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109784175:109784175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879C>T
AA Mutation	p.Pro627Ser(p.P627S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109783782:109783782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2272G>T
AA Mutation	p.Gly758Cys(p.G758C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109783643:109783643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2411G>T
AA Mutation	p.Ser804Ile(p.S804I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109782644:109782644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3410G>A
AA Mutation	p.Arg1137His(p.R1137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109784108:109784108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1946C>T
AA Mutation	p.Ala649Val(p.A649V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109784437:109784437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1617C>A
AA Mutation	p.Phe539Leu(p.F539L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109782531:109782531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3523G>A
AA Mutation	p.Ala1175Thr(p.A1175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375856
Start	109783662:109783662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767024195
CDS Mutation	c.2392G>A
AA Mutation	p.Val798Ile(p.V798I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375856
Start	109784272:109784272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1782G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375856
Start	109782805:109782805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3249G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375856
Start	109785277:109785277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRS2

No Mutation Annotation!