Colon Cancer: Gene >> IPO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9433785:9433785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2013G>C
AA Mutation	p.Met671Ile(p.M671I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9430891:9430891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1769A>C
AA Mutation	p.Gln590Pro(p.Q590P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9414325:9414325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550C>A
AA Mutation	p.Arg184Ser(p.R184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9435010:9435010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2151G>T
AA Mutation	p.Met717Ile(p.M717I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9437896:9437896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2411T>G
AA Mutation	p.Leu804Arg(p.L804R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9445183:9445183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3106G>T
AA Mutation	p.Gly1036Trp(p.G1036W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9410081:9410081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474T>A
AA Mutation	p.Asn158Lys(p.N158K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9420661:9420661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869A>G
AA Mutation	p.Glu290Gly(p.E290G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9437898:9437898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773555364
CDS Mutation	c.2413C>T
AA Mutation	p.Arg805Cys(p.R805C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9430899:9430899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1777C>A
AA Mutation	p.Gln593Lys(p.Q593K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379719
Start	9438170:9438170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2580G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379719
Start	9440460:9440460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2701C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379719
Start	9409982:9409982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379719
Start	9445143:9445143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3066A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379719
Start	9425208:9425208(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1287delA
AA Mutation	p.Asp430MetfsTer6(p.D430Mfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379719
Start	9429134:9429134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1531delA
AA Mutation	p.Met511CysfsTer3(p.M511Cfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000379719
Start	9420438:9420438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Ter(p.R252*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000379719
Start	9429133:9429133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528G>T
AA Mutation	p.Glu510Ter(p.E510*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000379719
Start	9436269:9436269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IPO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379719
Start	9420494:9420494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810A>C
AA Mutation	p.Arg270Ser(p.R270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379719
Start	9438110:9438110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2520A>G
Mutation Classification	Silent
Feature Type	Transcript