Colon Cancer: Gene >> INSM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35535117:35535117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>A
AA Mutation	p.Val289Ile(p.V289I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35535147:35535147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895G>A
AA Mutation	p.Val299Met(p.V299M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35535577:35535577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763893619
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442His(p.R442H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35534970:35534970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718A>G
AA Mutation	p.Lys240Glu(p.K240E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35534382:35534382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35535907:35535907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1655G>A
AA Mutation	p.Ser552Asn(p.S552N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307169
Start	35535257:35535257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746757298
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307169
Start	35535080:35535080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307169
Start	35535851:35535851(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1605delT
AA Mutation	p.Phe535LeufsTer6(p.F535Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307169
Start	35535850:35535851(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756928018
CDS Mutation	c.1605dupT
AA Mutation	p.Ser536Ter(p.S536*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> INSM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35535688:35535688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436T>C
AA Mutation	p.Phe479Ser(p.F479S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307169
Start	35535524:35535524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1272G>T
AA Mutation	p.Glu424Asp(p.E424D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307169
Start	35534990:35534990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>A
Mutation Classification	Silent
Feature Type	Transcript