Colon Cancer: Gene >> ITGA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52939886:52939886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3227C>A
AA Mutation	p.Ser1076Tyr(p.S1076Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52922831:52922831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150059220
CDS Mutation	c.2347G>A
AA Mutation	p.Asp783Asn(p.D783N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52910264:52910264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702G>A
AA Mutation	p.Gly568Arg(p.G568R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52918746:52918746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2003C>T
AA Mutation	p.Ala668Val(p.A668V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52849458:52849458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155A>G
AA Mutation	p.Gln52Arg(p.Q52R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52932129:52932129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2854T>C
AA Mutation	p.Phe952Leu(p.F952L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52910270:52910270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708C>T
AA Mutation	p.Arg570Cys(p.R570C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52849374:52849374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759463731
CDS Mutation	c.71G>A
AA Mutation	p.Arg24His(p.R24H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52898324:52898324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200911359
CDS Mutation	c.1250G>A
AA Mutation	p.Arg417Gln(p.R417Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52881969:52881969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721G>A
AA Mutation	p.Val241Ile(p.V241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52933987:52933987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2955C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52918807:52918807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2064C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52939598:52939598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52932113:52932113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2838T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52947449:52947449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3483A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282588
Start	52915500:52915500(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1899delT
AA Mutation	p.Phe633LeufsTer11(p.F633Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282588
Start	52918798:52918799(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2060dupA
AA Mutation	p.Asn687LysfsTer19(p.N687Kfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ITGA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52893767:52893767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>A
AA Mutation	p.Phe339Leu(p.F339L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52937417:52937417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2981C>A
AA Mutation	p.Ser994Tyr(p.S994Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282588
Start	52939913:52939913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139065570
CDS Mutation	c.3254C>T
AA Mutation	p.Ser1085Leu(p.S1085L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52898322:52898322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52915475:52915475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1869A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52939914:52939914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753899066
CDS Mutation	c.3255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282588
Start	52933987:52933987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2955C>A
Mutation Classification	Silent
Feature Type	Transcript