Colon Cancer: Gene >> AGMO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15418589:15418589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578A>C
AA Mutation	p.Asn193Thr(p.N193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000342526
Start	15385448:15385448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072G>A
AA Mutation	p.Ala358Thr(p.A358T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15390900:15390900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682A>C
AA Mutation	p.Asn228His(p.N228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15418577:15418577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590A>G
AA Mutation	p.Gln197Arg(p.Q197R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15560252:15560252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769378096
CDS Mutation	c.146C>A
AA Mutation	p.Ser49Tyr(p.S49Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15561796:15561796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746980089
CDS Mutation	c.50G>A
AA Mutation	p.Arg17His(p.R17H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342526
Start	15544833:15544833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536193303
CDS Mutation	c.348T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342526
Start	15560218:15560218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342526
Start	15366214:15366214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755873183
CDS Mutation	c.1083G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342526
Start	15385506:15385506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342526
Start	15387449:15387449(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.914delG
AA Mutation	p.Gly305ValfsTer31(p.G305Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000342526
Start	15561721:15561721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.125delA
AA Mutation	p.Lys42ArgfsTer9(p.K42Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000342526
Start	15387417:15387417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>T
AA Mutation	p.Glu316Ter(p.E316*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000342526
Start	15365600:15365601(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1176_1177insAAATGAAGTAGA
AA Mutation	p.Met392_Glu393insLysTerSerArg(p.M392_E393insK*SR)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000342526
Start	15561720:15561721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.125dupA
AA Mutation	p.Ala43GlyfsTer12(p.A43Gfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342526
Start	15390724:15390725(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.768dupA
AA Mutation	p.Val257SerfsTer10(p.V257Sfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AGMO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15387447:15387447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.916C>A
AA Mutation	p.Pro306Thr(p.P306T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342526
Start	15390900:15390900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682A>G
AA Mutation	p.Asn228Asp(p.N228D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript