Colon Cancer: Gene >> ITGB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44901658:44901658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575C>A
AA Mutation	p.Pro192His(p.P192H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44901695:44901695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574757270
CDS Mutation	c.538G>A
AA Mutation	p.Val180Met(p.V180M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44900400:44900400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852618
CDS Mutation	c.817G>A
AA Mutation	p.Gly273Arg(p.G273R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44900450:44900450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756545465
CDS Mutation	c.767C>T
AA Mutation	p.Thr256Met(p.T256M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44901595:44901595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638A>G
AA Mutation	p.Asn213Ser(p.N213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44910319:44910319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374031101
CDS Mutation	c.112G>A
AA Mutation	p.Glu38Lys(p.E38K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44900438:44900438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779T>C
AA Mutation	p.Val260Ala(p.V260A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44910354:44910354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148038936
CDS Mutation	c.77C>T
AA Mutation	p.Thr26Met(p.T26M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44901670:44901670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>A
AA Mutation	p.Arg188Gln(p.R188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44889396:44889396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757G>A
AA Mutation	p.Arg586Gln(p.R586Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44910770:44910770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737078
CDS Mutation	c.13C>T
AA Mutation	p.Arg5Cys(p.R5C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44899095:44899095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965T>C
AA Mutation	p.Val322Ala(p.V322A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44891983:44891983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1238T>C
AA Mutation	p.Val413Ala(p.V413A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44890142:44890142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369318947
CDS Mutation	c.1493G>A
AA Mutation	p.Arg498Gln(p.R498Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44891906:44891906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372056902
CDS Mutation	c.1315G>A
AA Mutation	p.Val439Met(p.V439M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44893455:44893455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747895476
CDS Mutation	c.1173G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44910732:44910732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768225440
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44900410:44900410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142381225
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44893485:44893485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1143C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44900401:44900401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779979379
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44903399:44903399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44907027:44907027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44906961:44906961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44888871:44888871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764303161
CDS Mutation	c.1902C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44899100:44899100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761463928
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302347
Start	44900389:44900389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147150938
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302347
Start	44906937:44906937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.306delA
AA Mutation	p.Val103Ter(p.V103*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000302347
Start	44890089:44890089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.Gln516Ter(p.Q516*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000302347
Start	44889344:44889344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1809C>A
AA Mutation	p.Cys603Ter(p.C603*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000302347
Start	44900319:44900319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201752283
CDS Mutation	c.897+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ITGB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44886774:44886774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568682818
CDS Mutation	c.2209C>T
AA Mutation	p.Arg737Cys(p.R737C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302347
Start	44886409:44886409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2269G>A
AA Mutation	p.Ala757Thr(p.A757T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000302347
Start	44903453:44903453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>A
AA Mutation	p.Tyr137Ter(p.Y137*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript