Colon Cancer: Gene >> HOMER2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304231
Start	82851219:82851219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>A
AA Mutation	p.Leu270Ile(p.L270I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304231
Start	82854691:82854691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637A>G
AA Mutation	p.Arg213Gly(p.R213G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304231
Start	82864175:82864175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379C>A
AA Mutation	p.His127Asn(p.H127N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304231
Start	82864238:82864238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>A
AA Mutation	p.Val106Met(p.V106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304231
Start	82892711:82892711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201320170
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Trp(p.R46W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304231
Start	82892815:82892815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757701596
CDS Mutation	c.32C>T
AA Mutation	p.Ala11Val(p.A11V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304231
Start	82864179:82864179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304231
Start	82892814:82892814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201522712
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304231
Start	82859121:82859121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760018246
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304231
Start	82864203:82864203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755349946
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000304231
Start	82852253:82852253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HOMER2

No Mutation Annotation!