Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GAB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154680172:154680172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604C>T
AA Mutation	p.Ala535Val(p.A535V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154678206:154678206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733G>T
AA Mutation	p.Trp578Leu(p.W578L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154695966:154695966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478T>G
AA Mutation	p.Phe493Cys(p.F493C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154716317:154716317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Cys(p.R29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154695965:154695965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1479T>G
AA Mutation	p.Phe493Leu(p.F493L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154678203:154678203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736C>T
AA Mutation	p.Thr579Met(p.T579M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154700026:154700026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100A>T
AA Mutation	p.Asp367Val(p.D367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369575
Start	154716149:154716149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147290916
CDS Mutation	c.253G>A
AA Mutation	p.Val85Met(p.V85M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369575
Start	154716063:154716063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369575
Start	154695923:154695923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369575
Start	154716150:154716150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369575
Start	154716113:154716113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000369575
Start	154697205:154697206(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1350_1351insTAAACCTCACC
AA Mutation	p.Pro451Ter(p.P451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_lost
Transcription ID	ENST00000369575
Start	154678179:154678179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1760G>C
AA Mutation	p.Ter587SerextTer54(p.587Sext54)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GAB3

No Mutation Annotation!