Colon Cancer: Gene >> AGBL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	49245833:49245833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314A>G
AA Mutation	p.Lys105Arg(p.K105R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	48534282:48534282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403C>T
AA Mutation	p.Ser468Phe(p.S468F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	48663193:48663193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577993447
CDS Mutation	c.683G>A
AA Mutation	p.Arg228Gln(p.R228Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	48634513:48634513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771499735
CDS Mutation	c.931G>A
AA Mutation	p.Val311Ile(p.V311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	48587121:48587121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Cys(p.R384C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	49245790:49245790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357A>T
AA Mutation	p.Lys119Asn(p.K119N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	49697363:49697363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369139471
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	48590915:48590915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752378443
CDS Mutation	c.1022A>G
AA Mutation	p.Asn341Ser(p.N341S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371839
Start	48653381:48653381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371839
Start	49045695:49045695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371839
Start	48634544:48634544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371839
Start	48534278:48534279(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1406_1407insACAAA
AA Mutation	p.Pro470GlnfsTer27(p.P470Qfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000371839
Start	48653453:48653453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575132944
CDS Mutation	c.725-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000371839
Start	48587002:48587002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AGBL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371839
Start	48634575:48634575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779103173
CDS Mutation	c.869G>A
AA Mutation	p.Arg290His(p.R290H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript