Colon Cancer: Gene >> GFRA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21705044:21705044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986G>A
AA Mutation	p.Gly329Glu(p.G329E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21750912:21750912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470A>C
AA Mutation	p.Lys157Thr(p.K157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21775032:21775032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379C>T
AA Mutation	p.Pro127Ser(p.P127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21702833:21702833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190G>C
AA Mutation	p.Ser397Thr(p.S397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21782798:21782798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142G>A
AA Mutation	p.Ala48Thr(p.A48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21705053:21705053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781276745
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21750879:21750879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503G>A
AA Mutation	p.Cys168Tyr(p.C168Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21704998:21704998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1032G>T
AA Mutation	p.Glu344Asp(p.E344D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21694477:21694477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1259T>C
AA Mutation	p.Met420Thr(p.M420T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21750684:21750684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698G>A
AA Mutation	p.Arg233His(p.R233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GFRA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517328
Start	21702951:21702951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072G>A
AA Mutation	p.Gly358Ser(p.G358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript