Colon Cancer: Gene >> ITGBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101692683:101692683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749949431
CDS Mutation	c.1114G>A
AA Mutation	p.Asp372Asn(p.D372N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101575522:101575522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Asp188Asn(p.D188N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101454095:101454095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Cys104Tyr(p.C104Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101598212:101598212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928T>C
AA Mutation	p.Cys310Arg(p.C310R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101567712:101567712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101575503:101575503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759757138
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101579321:101579321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101453934:101453934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ITGBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101583279:101583279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759322869
CDS Mutation	c.791T>C
AA Mutation	p.Ile264Thr(p.I264T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101706859:101706859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236G>T
AA Mutation	p.Lys412Asn(p.K412N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101579351:101579351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651A>C
AA Mutation	p.Glu217Asp(p.E217D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101567702:101567702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320A>G
AA Mutation	p.His107Arg(p.H107R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101583259:101583259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145784947
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript