Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SPRY1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123401834:123401834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243A>G
AA Mutation	p.Ile81Met(p.I81M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123401832:123401832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241A>G
AA Mutation	p.Ile81Val(p.I81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123401878:123401878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287A>G
AA Mutation	p.His96Arg(p.H96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123401639:123401639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>G
AA Mutation	p.Ile16Met(p.I16M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123401603:123401603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12A>C
AA Mutation	p.Gln4His(p.Q4H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339241
Start	123401840:123401840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000339241
Start	123402353:123402353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750666163
CDS Mutation	c.762C>A
AA Mutation	p.Cys254Ter(p.C254*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SPRY1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123402313:123402313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762280661
CDS Mutation	c.722A>G
AA Mutation	p.Tyr241Cys(p.Y241C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339241
Start	123401764:123401764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746376752
CDS Mutation	c.173C>T
AA Mutation	p.Ser58Leu(p.S58L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339241
Start	123402353:123402353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript