Colon Cancer: Gene >> ZNF138

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307355
Start	64831975:64831975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754223101
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Cys(p.R245C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307355
Start	64831679:64831679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437A>G
AA Mutation	p.Lys146Arg(p.K146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307355
Start	64831658:64831658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416T>C
AA Mutation	p.Phe139Ser(p.F139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307355
Start	64832103:64832103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307355
Start	64831989:64831989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF138

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307355
Start	64831693:64831693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451T>C
AA Mutation	p.Phe151Leu(p.F151L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307355
Start	64831719:64831719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477A>C
Mutation Classification	Silent
Feature Type	Transcript