Colon Cancer: Gene >> ASTE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131018607:131018607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412A>G
AA Mutation	p.Tyr471Cys(p.Y471C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131016297:131016297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556C>T
AA Mutation	p.Ala519Val(p.A519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131024826:131024826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481A>G
AA Mutation	p.Ser161Gly(p.S161G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264992
Start	131025007:131025007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264992
Start	131024799:131024799(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.508delA
AA Mutation	p.Thr170LeufsTer6(p.T170Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000264992
Start	131024241:131024241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066C>T
AA Mutation	p.Gln356Ter(p.Q356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ASTE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131024858:131024858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449A>G
AA Mutation	p.Asn150Ser(p.N150S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131014259:131014259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1838C>T
AA Mutation	p.Ser613Leu(p.S613L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131025256:131025256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51C>A
AA Mutation	p.Phe17Leu(p.F17L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264992
Start	131025118:131025118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200808262
CDS Mutation	c.189C>A
AA Mutation	p.Phe63Leu(p.F63L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000264992
Start	131024454:131024454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773437504
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Ter(p.R285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000264992
Start	131024834:131024834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473C>A
AA Mutation	p.Ser158Ter(p.S158*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript