Colon Cancer: Gene >> MEOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262041
Start	15626912:15626912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524A>T
AA Mutation	p.Gln175Leu(p.Q175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262041
Start	15685913:15685913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141784602
CDS Mutation	c.490G>A
AA Mutation	p.Gly164Ser(p.G164S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262041
Start	15685933:15685933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262041
Start	15686115:15686115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753470533
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262041
Start	15612558:15612558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262041
Start	15686313:15686313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262041
Start	15686050:15686050(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.353delC
AA Mutation	p.Pro118GlnfsTer98(p.P118Qfs*98)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MEOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262041
Start	15686264:15686264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139T>C
AA Mutation	p.Ser47Pro(p.S47P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000262041
Start	15626847:15626847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>T
AA Mutation	p.Glu197Ter(p.E197*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript