Colon Cancer: Gene >> SOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325404
Start	181713198:181713198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>A
AA Mutation	p.Gly280Ser(p.G280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325404
Start	181713004:181713004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644C>T
AA Mutation	p.Thr215Ile(p.T215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325404
Start	181712561:181712561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>A
AA Mutation	p.His67Gln(p.H67Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325404
Start	181712520:181712520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Gly54Arg(p.G54R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325404
Start	181713189:181713189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829T>C
AA Mutation	p.Tyr277His(p.Y277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325404
Start	181712962:181712962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602A>G
AA Mutation	p.Asp201Gly(p.D201G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325404
Start	181713050:181713050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325404
Start	181712789:181712789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325404
Start	181712420:181712420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325404
Start	181712588:181712588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SOX2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325404
Start	181713272:181713272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.912C>A
Mutation Classification	Silent
Feature Type	Transcript