Colon Cancer: Gene >> GFRA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319242
Start	3660586:3660586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Gly223Arg(p.G223R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319242
Start	3660664:3660664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768661396
CDS Mutation	c.589G>A
AA Mutation	p.Ala197Thr(p.A197T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319242
Start	3660217:3660217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760C>T
AA Mutation	p.Pro254Ser(p.P254S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319242
Start	3660566:3660566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000319242
Start	3660565:3660565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>T
AA Mutation	p.Glu230Ter(p.E230*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GFRA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319242
Start	3660246:3660246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731G>A
AA Mutation	p.Gly244Asp(p.G244D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript