Colon Cancer: Gene >> HOMER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334082
Start	79456948:79456948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76C>T
AA Mutation	p.Pro26Ser(p.P26S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334082
Start	79402045:79402045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538A>G
AA Mutation	p.Ser180Gly(p.S180G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334082
Start	79451014:79451014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270C>A
AA Mutation	p.Phe90Leu(p.F90L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334082
Start	79447060:79447060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380C>A
AA Mutation	p.Pro127His(p.P127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334082
Start	79457003:79457003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334082
Start	79451113:79451113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334082
Start	79450993:79450993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334082
Start	79439144:79439144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745316039
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HOMER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334082
Start	79447124:79447124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316T>G
AA Mutation	p.Phe106Val(p.F106V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript