Colon Cancer: Gene >> STRADA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000336174
Start	63710728:63710728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768734514
CDS Mutation	c.457G>A
AA Mutation	p.Gly153Ser(p.G153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336174
Start	63703669:63703669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226A>G
AA Mutation	p.Gln409Arg(p.Q409R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336174
Start	63704558:63704558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883A>T
AA Mutation	p.Thr295Ser(p.T295S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336174
Start	63703640:63703640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773110344
CDS Mutation	c.1255A>G
AA Mutation	p.Thr419Ala(p.T419A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336174
Start	63726675:63726675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57C>A
AA Mutation	p.Phe19Leu(p.F19L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336174
Start	63710795:63710795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336174
Start	63703644:63703644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336174
Start	63707401:63707401(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.599delA
AA Mutation	p.His200ProfsTer3(p.H200Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336174
Start	63704444:63704444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762120842
CDS Mutation	c.997delC
AA Mutation	p.Arg333GlyfsTer42(p.R333Gfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STRADA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336174
Start	63707287:63707287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713T>A
AA Mutation	p.Val238Asp(p.V238D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336174
Start	63710559:63710559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779411398
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript