Colon Cancer: Gene >> GET4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265857
Start	891003:891003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542A>G
AA Mutation	p.Glu181Gly(p.E181G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265857
Start	892357:892357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754748449
CDS Mutation	c.685G>A
AA Mutation	p.Gly229Arg(p.G229R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265857
Start	886087:886087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759801442
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Trp(p.R63W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265857
Start	891031:891031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374735615
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GET4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265857
Start	886588:886588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254T>C
AA Mutation	p.Leu85Ser(p.L85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265857
Start	895395:895395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144524340
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265857
Start	887419:887419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191613326
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript