Colon Cancer: Gene >> ELF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34480804:34480804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669A>T
AA Mutation	p.Arg223Ser(p.R223S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34493487:34493487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34493521:34493521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778628535
CDS Mutation	c.343G>A
AA Mutation	p.Gly115Ser(p.G115S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34480959:34480959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514A>C
AA Mutation	p.Ser172Arg(p.S172R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34493539:34493539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773417409
CDS Mutation	c.325G>A
AA Mutation	p.Glu109Lys(p.E109K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34505700:34505700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80G>A
AA Mutation	p.Cys27Tyr(p.C27Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34480814:34480814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659A>C
AA Mutation	p.Lys220Thr(p.K220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000312319
Start	34511543:34511543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ELF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34480932:34480932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Asp181Asn(p.D181N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312319
Start	34490045:34490045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400A>C
AA Mutation	p.Asn134His(p.N134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript