Colon Cancer: Gene >> TMEM140

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275767
Start	135164448:135164448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776496054
CDS Mutation	c.7G>A
AA Mutation	p.Gly3Ser(p.G3S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275767
Start	135164677:135164677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236G>A
AA Mutation	p.Gly79Asp(p.G79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275767
Start	135164829:135164829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150916088
CDS Mutation	c.388G>A
AA Mutation	p.Gly130Ser(p.G130S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275767
Start	135164882:135164882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199612642
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275767
Start	135164795:135164795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275767
Start	135164921:135164921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000275767
Start	135164731:135164731(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.295delC
AA Mutation	p.Gln99SerfsTer5(p.Q99Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM140

No Mutation Annotation!