Colon Cancer: Gene >> DPP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154887726:154887726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2296G>A
AA Mutation	p.Ala766Thr(p.A766T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154794179:154794179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237G>A
AA Mutation	p.Ala413Thr(p.A413T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154803896:154803896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1440C>G
AA Mutation	p.Ile480Met(p.I480M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154669430:154669430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751G>T
AA Mutation	p.Gly251Cys(p.G251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154794176:154794176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234G>A
AA Mutation	p.Asp412Asn(p.D412N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154887711:154887711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2281G>A
AA Mutation	p.Gly761Arg(p.G761R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404039
Start	153887711:153887711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>A
AA Mutation	p.Ala10Thr(p.A10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154804952:154804952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1535G>T
AA Mutation	p.Arg512Leu(p.R512L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154807048:154807048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1602G>T
AA Mutation	p.Glu534Asp(p.E534D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377770
Start	154801462:154801462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1407G>T
AA Mutation	p.Gln469His(p.Q469H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154475034:154475034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454A>C
AA Mutation	p.Ser152Arg(p.S152R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154727797:154727797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793T>G
AA Mutation	p.Cys265Gly(p.C265G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154769456:154769456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537661099
CDS Mutation	c.923C>T
AA Mutation	p.Pro308Leu(p.P308L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154889341:154889341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745885265
CDS Mutation	c.2374G>A
AA Mutation	p.Asp792Asn(p.D792N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154769438:154769438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905T>A
AA Mutation	p.Ile302Asn(p.I302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154875962:154875962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546439141
CDS Mutation	c.1940C>T
AA Mutation	p.Thr647Met(p.T647M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154876028:154876028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2006G>T
AA Mutation	p.Gly669Val(p.G669V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154669425:154669425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746C>A
AA Mutation	p.Pro249His(p.P249H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154892463:154892463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2581G>A
AA Mutation	p.Asp861Asn(p.D861N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154876005:154876005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372493523
CDS Mutation	c.1983C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154876017:154876017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558465693
CDS Mutation	c.1995C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154892411:154892411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154769481:154769481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369459411
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154794124:154794124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757195104
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000377770
Start	154853821:154853825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1711_1714+1delAAAAG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377770
Start	154540617:154540618(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.550dupA
AA Mutation	p.Ile184AsnfsTer2(p.I184Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000377770
Start	154801464:154801464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1407+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DPP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154540579:154540579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505A>G
AA Mutation	p.Asn169Asp(p.N169D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154794114:154794114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172G>A
AA Mutation	p.Ser391Asn(p.S391N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377770
Start	154892428:154892428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2546T>C
AA Mutation	p.Ile849Thr(p.I849T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154892456:154892456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115455867
CDS Mutation	c.2574G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377770
Start	154795850:154795850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377039321
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript