Colon Cancer: Gene >> RSPO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356545
Start	37614312:37614312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308A>G
AA Mutation	p.Glu103Gly(p.E103G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356545
Start	37629618:37629618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756170881
CDS Mutation	c.44C>T
AA Mutation	p.Thr15Met(p.T15M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356545
Start	37629657:37629657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377442675
CDS Mutation	c.5G>A
AA Mutation	p.Arg2Gln(p.R2Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356545
Start	37613748:37613748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581A>G
AA Mutation	p.Lys194Arg(p.K194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356545
Start	37613892:37613892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761409987
CDS Mutation	c.437C>T
AA Mutation	p.Ala146Val(p.A146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RSPO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356545
Start	37616502:37616502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>A
AA Mutation	p.Asp90Asn(p.D90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript