Colon Cancer: Gene >> BIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316724
Start	127052317:127052317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309G>A
AA Mutation	p.Ala437Thr(p.A437T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316724
Start	127068997:127068997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446A>G
AA Mutation	p.Asp149Gly(p.D149G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316724
Start	127051203:127051203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746346952
CDS Mutation	c.1412C>T
AA Mutation	p.Ala471Val(p.A471V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316724
Start	127048561:127048561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759691190
CDS Mutation	c.1747G>A
AA Mutation	p.Val583Ile(p.V583I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316724
Start	127050477:127050477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1618C>A
AA Mutation	p.Gln540Lys(p.Q540K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316724
Start	127053941:127053941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316724
Start	127052285:127052285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316724
Start	127068225:127068225(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.550delC
AA Mutation	p.Gln184SerfsTer12(p.Q184Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BIN1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316724
Start	127053917:127053917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751173050
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316724
Start	127052345:127052345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373834859
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript