Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DPP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115791103:115791103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554T>A
AA Mutation	p.Asn518Lys(p.N518K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115815701:115815701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922A>G
AA Mutation	p.Asp641Gly(p.D641G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115840791:115840791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224C>A
AA Mutation	p.Leu742Ile(p.L742I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115791161:115791161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1612C>A
AA Mutation	p.Leu538Ile(p.L538I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115791329:115791329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371613510
CDS Mutation	c.1673G>A
AA Mutation	p.Arg558Gln(p.R558Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115836251:115836251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2045T>C
AA Mutation	p.Leu682Ser(p.L682S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115762584:115762584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087A>T
AA Mutation	p.Thr363Ser(p.T363S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115739844:115739844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148038008
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115525964:115525964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566062096
CDS Mutation	c.433G>A
AA Mutation	p.Val145Ile(p.V145I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115836223:115836223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764715614
CDS Mutation	c.2017G>A
AA Mutation	p.Val673Met(p.V673M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115309341:115309341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163C>T
AA Mutation	p.Leu55Phe(p.L55F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115727907:115727907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668T>C
AA Mutation	p.Phe223Ser(p.F223S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115768325:115768325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142G>A
AA Mutation	p.Gly381Asp(p.G381D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115525961:115525961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Asp144Asn(p.D144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115815707:115815707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1928A>G
AA Mutation	p.Lys643Arg(p.K643R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115836184:115836184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1978A>G
AA Mutation	p.Ile660Val(p.I660V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115309267:115309267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89G>T
AA Mutation	p.Arg30Ile(p.R30I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115739788:115739788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371206408
CDS Mutation	c.747A>C
AA Mutation	p.Glu249Asp(p.E249D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115836735:115836735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2171G>A
AA Mutation	p.Gly724Glu(p.G724E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115791304:115791304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648T>C
AA Mutation	p.Ser550Pro(p.S550P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115689700:115689700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455C>T
AA Mutation	p.Ser152Leu(p.S152L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115499601:115499601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115814941:115814941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115739761:115739761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753852164
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115791118:115791118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000410059
Start	115777293:115777293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1312delA
AA Mutation	p.Ile438PhefsTer4(p.I438Ffs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000410059
Start	115777245:115777245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259C>A
AA Mutation	p.Ser420Ter(p.S420*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000410059
Start	115777790:115777791(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1320dupT
AA Mutation	p.Leu441SerfsTer4(p.L441Sfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000410059
Start	115525897:115525897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DPP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115689880:115689880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>A
AA Mutation	p.Val179Ile(p.V179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115727889:115727889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650G>A
AA Mutation	p.Gly217Glu(p.G217E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115791329:115791329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371613510
CDS Mutation	c.1673G>A
AA Mutation	p.Arg558Gln(p.R558Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115727874:115727874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764618439
CDS Mutation	c.635G>A
AA Mutation	p.Arg212Gln(p.R212Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115780879:115780879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367C>G
AA Mutation	p.Ser456Cys(p.S456C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115791307:115791307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651C>T
AA Mutation	p.Leu551Phe(p.L551F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115499546:115499546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308T>A
AA Mutation	p.Val103Asp(p.V103D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115777831:115777831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358A>G
AA Mutation	p.Tyr453Cys(p.Y453C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115525934:115525934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403G>T
AA Mutation	p.Asp135Tyr(p.D135Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115777266:115777266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280A>T
AA Mutation	p.Lys427Met(p.K427M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000410059
Start	115836173:115836173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1967T>A
AA Mutation	p.Ile656Asn(p.I656N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115739789:115739789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115814859:115814859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410059
Start	115739866:115739866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000410059
Start	115814941:115814941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849C>T
AA Mutation	p.Arg617Ter(p.R617*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000410059
Start	115836710:115836710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2146G>T
AA Mutation	p.Glu716Ter(p.E716*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript