Colon Cancer: Gene >> ITGA2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44385324:44385324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Cys(p.R196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383631:44383631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072C>T
AA Mutation	p.Arg358Cys(p.R358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383606:44383606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764585011
CDS Mutation	c.1097G>A
AA Mutation	p.Arg366Gln(p.R366Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383595:44383595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108G>A
AA Mutation	p.Ala370Thr(p.A370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383679:44383679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024C>T
AA Mutation	p.Pro342Ser(p.P342S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44372408:44372408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3076C>T
AA Mutation	p.Arg1026Trp(p.R1026W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44380989:44380989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1283A>G
AA Mutation	p.Glu428Gly(p.E428G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44385052:44385052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383942:44383942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752213788
CDS Mutation	c.950C>T
AA Mutation	p.Ala317Val(p.A317V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44383908:44383908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44380638:44380638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766997708
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44375100:44375100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766712350
CDS Mutation	c.2739G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44377065:44377065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752778097
CDS Mutation	c.2211C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44378455:44378455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184333409
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44376313:44376313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2343G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44383521:44383521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44384578:44384578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44386113:44386113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375882355
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44378675:44378675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1914A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44384560:44384560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44377080:44377080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2196C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000262407
Start	44384964:44384964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783C>A
AA Mutation	p.Tyr261Ter(p.Y261*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ITGA2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44380928:44380928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1344T>G
AA Mutation	p.Phe448Leu(p.F448L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44383508:44383508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Trp(p.R399W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44380434:44380434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1496C>A
AA Mutation	p.Pro499His(p.P499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262407
Start	44376359:44376359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2297T>G
AA Mutation	p.Ile766Ser(p.I766S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44384961:44384961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262407
Start	44378702:44378702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1887C>T
Mutation Classification	Silent
Feature Type	Transcript