Colon Cancer: Gene >> ITGB5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124763711:124763711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2312A>C
AA Mutation	p.Asn771Thr(p.N771T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124821405:124821405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776835945
CDS Mutation	c.850G>A
AA Mutation	p.Ala284Thr(p.A284T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124848489:124848489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431T>C
AA Mutation	p.Met144Thr(p.M144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124859247:124859247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356G>T
AA Mutation	p.Arg119Leu(p.R119L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124773793:124773793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813C>T
AA Mutation	p.Arg605Cys(p.R605C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124859391:124859391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212T>C
AA Mutation	p.Val71Ala(p.V71A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296181
Start	124764418:124764418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199862649
CDS Mutation	c.2277C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296181
Start	124796695:124796695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775683311
CDS Mutation	c.1386G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296181
Start	124796599:124796599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296181
Start	124773878:124773878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144048165
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296181
Start	124819757:124819758(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs763839738
CDS Mutation	c.1019dupA
AA Mutation	p.Asn340LysfsTer34(p.N340Kfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000296181
Start	124873445:124873445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ITGB5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296181
Start	124809123:124809123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1162G>T
AA Mutation	p.Asp388Tyr(p.D388Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296181
Start	124859441:124859441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777220294
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript