Colon Cancer: Gene >> ITGB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32910381:32910381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006A>T
AA Mutation	p.Asn669Ile(p.N669I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32908389:32908389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2310A>C
AA Mutation	p.Lys770Asn(p.K770N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32920065:32920065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289T>C
AA Mutation	p.Ile430Thr(p.I430T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32922288:32922288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097A>G
AA Mutation	p.Asn366Ser(p.N366S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32911953:32911953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1641T>G
AA Mutation	p.Ile547Met(p.I547M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32928153:32928153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488A>C
AA Mutation	p.Lys163Thr(p.K163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32928192:32928192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449A>G
AA Mutation	p.Asp150Gly(p.D150G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32911649:32911649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201856355
CDS Mutation	c.1730G>A
AA Mutation	p.Arg577His(p.R577H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32935542:32935542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17T>G
AA Mutation	p.Ile6Ser(p.I6S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32910255:32910255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2132A>G
AA Mutation	p.Asn711Ser(p.N711S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32922723:32922723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201869797
CDS Mutation	c.955A>G
AA Mutation	p.Ile319Val(p.I319V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32928169:32928169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472G>A
AA Mutation	p.Asp158Asn(p.D158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32920354:32920354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160G>A
AA Mutation	p.Gly387Asp(p.G387D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302278
Start	32929928:32929928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270G>T
AA Mutation	p.Lys90Asn(p.K90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302278
Start	32901588:32901588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201353781
CDS Mutation	c.2379G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302278
Start	32929922:32929922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302278
Start	32932533:32932533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200000349
CDS Mutation	c.135T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302278
Start	32911603:32911603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302278
Start	32929886:32929886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000302278
Start	32908440:32908441(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2258_2259insAGAAAGGAC
AA Mutation	p.Leu753_Leu754insGluArgThr(p.L753_L754insERT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ITGB1

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302278
Start	32920041:32920041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1313delA
AA Mutation	p.Lys438ArgfsTer17(p.K438Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript