Colon Cancer: Gene >> DACT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645381:58645381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758A>C
AA Mutation	p.Lys253Thr(p.K253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645634:58645634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011A>C
AA Mutation	p.Lys337Asn(p.K337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58647093:58647093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2470C>T
AA Mutation	p.Arg824Cys(p.R824C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646563:58646563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1940C>T
AA Mutation	p.Ala647Val(p.A647V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645311:58645311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>T
AA Mutation	p.Gly230Trp(p.G230W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646271:58646271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>A
AA Mutation	p.Glu550Lys(p.E550K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646775:58646775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147227144
CDS Mutation	c.2152G>A
AA Mutation	p.Ala718Thr(p.A718T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645453:58645453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830C>T
AA Mutation	p.Ala277Val(p.A277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645462:58645462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839G>A
AA Mutation	p.Ser280Asn(p.S280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58641596:58641596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483T>G
AA Mutation	p.Phe161Leu(p.F161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645671:58645671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048A>G
AA Mutation	p.Thr350Ala(p.T350A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58638522:58638522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320A>G
AA Mutation	p.Asn107Ser(p.N107S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646305:58646305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1682C>T
AA Mutation	p.Pro561Leu(p.P561L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646669:58646669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776830128
CDS Mutation	c.2046G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646438:58646438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1815G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646795:58646795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767912076
CDS Mutation	c.2172C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646774:58646774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760763089
CDS Mutation	c.2151C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58645361:58645361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335867
Start	58645665:58645665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1048delA
AA Mutation	p.Thr350HisfsTer4(p.T350Hfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335867
Start	58646177:58646177(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1559delC
AA Mutation	p.Pro520ArgfsTer60(p.P520Rfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000335867
Start	58646979:58646979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2356C>T
AA Mutation	p.Gln786Ter(p.Q786*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000335867
Start	58645887:58645887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>T
AA Mutation	p.Glu422Ter(p.E422*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DACT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645749:58645749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126G>A
AA Mutation	p.Val376Ile(p.V376I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645782:58645782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>A
AA Mutation	p.Gly387Ser(p.G387S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645314:58645314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645807:58645807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776160196
CDS Mutation	c.1184C>T
AA Mutation	p.Ser395Leu(p.S395L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646921:58646921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781117085
CDS Mutation	c.2298C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646174:58646174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646885:58646885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript