Colon Cancer: Gene >> SPRY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155774325:155774325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775484840
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155774491:155774491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620C>T
AA Mutation	p.Ala207Val(p.A207V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155774372:155774372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>G
AA Mutation	p.Cys167Trp(p.C167W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155774337:155774337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377355763
CDS Mutation	c.466G>A
AA Mutation	p.Val156Ile(p.V156I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155774638:155774638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771224871
CDS Mutation	c.767G>A
AA Mutation	p.Arg256Gln(p.R256Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155773926:155773926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779201129
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Cys(p.R19C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155774197:155774197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326G>T
AA Mutation	p.Gly109Val(p.G109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302805
Start	155773970:155773970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPRY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302805
Start	155773926:155773926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779201129
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Cys(p.R19C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript