Colon Cancer: Gene >> NAA15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139336917:139336917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209G>A
AA Mutation	p.Arg70His(p.R70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139388037:139388037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2554A>G
AA Mutation	p.Asn852Asp(p.N852D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139342926:139342926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503C>T
AA Mutation	p.Ala168Val(p.A168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139361866:139361866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1682C>A
AA Mutation	p.Ala561Asp(p.A561D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139351194:139351194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815A>T
AA Mutation	p.Asn272Ile(p.N272I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139370291:139370291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1834A>G
AA Mutation	p.Lys612Glu(p.K612E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139351586:139351586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989G>T
AA Mutation	p.Arg330Ile(p.R330I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139384859:139384859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2183A>C
AA Mutation	p.Asp728Ala(p.D728A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139361746:139361746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562A>G
AA Mutation	p.Asp521Gly(p.D521G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139361860:139361860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1676G>A
AA Mutation	p.Arg559Lys(p.R559K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139349578:139349578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>T
AA Mutation	p.Pro270Ser(p.P270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296543
Start	139378759:139378759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2060A>C
AA Mutation	p.Lys687Thr(p.K687T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296543
Start	139336909:139336909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296543
Start	139351533:139351533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296543
Start	139334200:139334200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296543
Start	139370291:139370291(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1841delA
AA Mutation	p.Asn614MetfsTer22(p.N614Mfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000296543
Start	139376383:139376383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966G>T
AA Mutation	p.Glu656Ter(p.E656*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000296543
Start	139342826:139342826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403G>T
AA Mutation	p.Glu135Ter(p.E135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000296543
Start	139361829:139361829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Ter(p.R549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000296543
Start	139357523:139357523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1225G>T
AA Mutation	p.Glu409Ter(p.E409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000296543
Start	139359741:139359741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NAA15

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000296543
Start	139370282:139370282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1825G>T
AA Mutation	p.Glu609Ter(p.E609*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000296543
Start	139386174:139386174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2344C>T
AA Mutation	p.Arg782Ter(p.R782*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript