Colon Cancer: Gene >> ITGA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181522286:181522286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199911081
CDS Mutation	c.2018C>T
AA Mutation	p.Thr673Met(p.T673M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181531692:181531692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2700C>A
AA Mutation	p.Phe900Leu(p.F900L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181529602:181529602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2492C>A
AA Mutation	p.Ser831Tyr(p.S831Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181458210:181458210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212C>T
AA Mutation	p.Ala71Val(p.A71V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181531675:181531675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2683C>T
AA Mutation	p.Pro895Ser(p.P895S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181457697:181457697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745388020
CDS Mutation	c.43G>A
AA Mutation	p.Ala15Thr(p.A15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181482623:181482623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013G>A
AA Mutation	p.Arg338Lys(p.R338K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181482544:181482544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>T
AA Mutation	p.Ala312Ser(p.A312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181482614:181482614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004A>G
AA Mutation	p.Glu335Gly(p.E335G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181457774:181457774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>A
AA Mutation	p.Ser40Arg(p.S40R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181480157:181480157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181457696:181457696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181485967:181485967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199782465
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181457744:181457744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181475182:181475182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181529624:181529624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2514G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000397033
Start	181480254:181480254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>T
AA Mutation	p.Gly248Ter(p.G248*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000397033
Start	181509733:181509733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753898074
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Ter(p.R591*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397033
Start	181509798:181509799(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1843dupA
AA Mutation	p.Thr615AsnfsTer11(p.T615Nfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000397033
Start	181524252:181524252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2249+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ITGA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181495386:181495386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355C>T
AA Mutation	p.Ala452Val(p.A452V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181475162:181475162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430T>G
AA Mutation	p.Cys144Gly(p.C144G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181531661:181531661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2669G>T
AA Mutation	p.Cys890Phe(p.C890F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181531746:181531746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2754A>T
AA Mutation	p.Gln918His(p.Q918H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181493376:181493376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205T>G
AA Mutation	p.Ile402Ser(p.I402S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181529602:181529602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2492C>A
AA Mutation	p.Ser831Tyr(p.S831Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181495903:181495903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506C>A
AA Mutation	p.Phe502Leu(p.F502L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397033
Start	181531692:181531692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2700C>A
AA Mutation	p.Phe900Leu(p.F900L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181457699:181457699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201902294
CDS Mutation	c.45C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181475212:181475212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397033
Start	181481641:181481641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201838862
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397033
Start	181509798:181509798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1836delG
AA Mutation	p.Met612IlefsTer5(p.M612Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript