Colon Cancer: Gene >> GRB10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398812
Start	50669733:50669733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772801673
CDS Mutation	c.493G>A
AA Mutation	p.Ala165Thr(p.A165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398812
Start	50593059:50593059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1678G>A
AA Mutation	p.Gly560Arg(p.G560R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398812
Start	50604356:50604356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411A>G
AA Mutation	p.Ile471Val(p.I471V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000398812
Start	50674658:50674658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140A>G
AA Mutation	p.Glu47Gly(p.E47G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398812
Start	50619199:50619199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745633042
CDS Mutation	c.748G>A
AA Mutation	p.Ala250Thr(p.A250T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398812
Start	50618093:50618093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555920373
CDS Mutation	c.824G>A
AA Mutation	p.Gly275Asp(p.G275D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398812
Start	50619217:50619217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730C>A
AA Mutation	p.Leu244Ile(p.L244I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398812
Start	50619197:50619197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398812
Start	50618107:50618107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GRB10

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398812
Start	50605302:50605302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377C>T
Mutation Classification	Silent
Feature Type	Transcript