Colon Cancer: Gene >> ITGB4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000200181
Start	75739705:75739705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2254G>A
AA Mutation	p.Gly752Ser(p.G752S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75743721:75743721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772928070
CDS Mutation	c.2971G>A
AA Mutation	p.Val991Met(p.V991M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75743757:75743757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3007C>T
AA Mutation	p.Arg1003Cys(p.R1003C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75757078:75757078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5189G>A
AA Mutation	p.Gly1730Asp(p.G1730D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75737409:75737409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078G>A
AA Mutation	p.Gly693Glu(p.G693E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000200181
Start	75729435:75729435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.737C>T
AA Mutation	p.Thr246Met(p.T246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000200181
Start	75743713:75743713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2963C>A
AA Mutation	p.Ala988Asp(p.A988D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75757089:75757089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5200A>G
AA Mutation	p.Ile1734Val(p.I1734V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75752315:75752315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3935C>T
AA Mutation	p.Ala1312Val(p.A1312V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75729292:75729292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594C>A
AA Mutation	p.Asp198Glu(p.D198E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75756996:75756996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149353166
CDS Mutation	c.5107G>A
AA Mutation	p.Val1703Met(p.V1703M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75750797:75750797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751047725
CDS Mutation	c.3592G>A
AA Mutation	p.Ala1198Thr(p.A1198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75740441:75740441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149608383
CDS Mutation	c.2530C>T
AA Mutation	p.Arg844Cys(p.R844C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75728419:75728419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512T>C
AA Mutation	p.Phe171Ser(p.F171S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75742374:75742374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2667G>T
AA Mutation	p.Met889Ile(p.M889I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75727436:75727436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372797886
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75730282:75730282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75751077:75751077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376494263
CDS Mutation	c.3759C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75743849:75743849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145314226
CDS Mutation	c.3099G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75754811:75754811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4554C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75757288:75757288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145897252
CDS Mutation	c.5307C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75742664:75742664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780448706
CDS Mutation	c.2865C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75752525:75752525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762937846
CDS Mutation	c.4056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75728402:75728402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75092172
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200181
Start	75750154:75750154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3360G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200181
Start	75757046:75757052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5159_5165delCCACTGA
AA Mutation	p.Thr1720ArgfsTer13(p.T1720Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200181
Start	75752287:75752287(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3910delG
AA Mutation	p.Ala1304ProfsTer140(p.A1304Pfs*140)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200181
Start	75737326:75737326(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1996delG
AA Mutation	p.Glu666ArgfsTer103(p.E666Rfs*103)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200181
Start	75750158:75750158(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3368delC
AA Mutation	p.Pro1123LeufsTer37(p.P1123Lfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200181
Start	75729291:75729292(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs752657203
CDS Mutation	c.600dupC
AA Mutation	p.Phe201LeufsTer15(p.F201Lfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ITGB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75733637:75733637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>C
AA Mutation	p.Gln534His(p.Q534H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75742463:75742463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2756G>A
AA Mutation	p.Gly919Asp(p.G919D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75736143:75736143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750G>T
AA Mutation	p.Asp584Tyr(p.D584Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000200181
Start	75752344:75752344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3964A>G
AA Mutation	p.Arg1322Gly(p.R1322G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript