Colon Cancer: Gene >> AXL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41256535:41256535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2120G>A
AA Mutation	p.Arg707His(p.R707H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41242973:41242973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403C>T
AA Mutation	p.Ala468Val(p.A468V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41237978:41237978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374699228
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41243687:41243687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41243009:41243009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751855310
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480His(p.R480H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41222039:41222039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41256577:41256577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2162T>C
AA Mutation	p.Leu721Pro(p.L721P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41242910:41242910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774958319
CDS Mutation	c.1340C>T
AA Mutation	p.Ser447Leu(p.S447L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41259570:41259570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201956398
CDS Mutation	c.2351G>A
AA Mutation	p.Arg784Gln(p.R784Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41252379:41252379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1740G>T
AA Mutation	p.Glu580Asp(p.E580D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41238037:41238037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>A
AA Mutation	p.Gln293Lys(p.Q293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41243668:41243668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144824336
CDS Mutation	c.1498G>A
AA Mutation	p.Val500Met(p.V500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41230977:41230977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597G>T
AA Mutation	p.Lys199Asn(p.K199N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41248526:41248526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550G>A
AA Mutation	p.Gly517Asp(p.G517D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41248534:41248534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1558G>A
AA Mutation	p.Glu520Lys(p.E520K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41252923:41252923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1882C>A
AA Mutation	p.Leu628Ile(p.L628I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41243004:41243004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434G>T
AA Mutation	p.Glu478Asp(p.E478D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41239302:41239302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273G>A
AA Mutation	p.Ala425Thr(p.A425T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41231245:41231245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301178
Start	41222016:41222016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769038891
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301178
Start	41220640:41220640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201764420
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301178
Start	41238480:41238480(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1010delC
AA Mutation	p.Pro337LeufsTer29(p.P337Lfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301178
Start	41238028:41238028(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.874delC
AA Mutation	p.His292IlefsTer5(p.H292Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AXL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41259671:41259671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763066660
CDS Mutation	c.2452G>A
AA Mutation	p.Glu818Lys(p.E818K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript