Colon Cancer: Gene >> AGAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57731924:57731924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1838C>T
AA Mutation	p.Pro613Leu(p.P613L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57728333:57728333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2602A>C
AA Mutation	p.Asn868His(p.N868H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57732874:57732874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1655G>A
AA Mutation	p.Gly552Glu(p.G552E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57731837:57731837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1925C>A
AA Mutation	p.Ala642Glu(p.A642E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57727767:57727767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2771G>A
AA Mutation	p.Arg924His(p.R924H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57726692:57726692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3439G>C
AA Mutation	p.Gly1147Arg(p.G1147R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57730830:57730830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2269G>A
AA Mutation	p.Val757Ile(p.V757I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57731639:57731639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957C>T
AA Mutation	p.Arg653Cys(p.R653C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57730881:57730881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2218C>T
AA Mutation	p.Pro740Ser(p.P740S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57732893:57732893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1636G>A
AA Mutation	p.Glu546Lys(p.E546K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547588
Start	57727554:57727554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2886C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547588
Start	57727064:57727064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777926635
CDS Mutation	c.3246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547588
Start	57727539:57727539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2901C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547588
Start	57730852:57730852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2247C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000547588
Start	57734387:57734387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333G>T
AA Mutation	p.Glu445Ter(p.E445*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57727420:57727420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3020C>T
AA Mutation	p.Ala1007Val(p.A1007V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57727412:57727412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3028G>A
AA Mutation	p.Val1010Met(p.V1010M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57730525:57730525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398G>T
AA Mutation	p.Asp800Tyr(p.D800Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57734074:57734074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501C>T
AA Mutation	p.Arg501Cys(p.R501C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000547588
Start	57731618:57731618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1978A>G
AA Mutation	p.Lys660Glu(p.K660E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000547588
Start	57727413:57727413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3027C>T
Mutation Classification	Silent
Feature Type	Transcript