Colon Cancer: Gene >> DIAPH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96945574:96945574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492G>A
AA Mutation	p.Ala498Thr(p.A498T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97075188:97075188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2174G>A
AA Mutation	p.Arg725His(p.R725H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96738593:96738593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747854335
CDS Mutation	c.173G>A
AA Mutation	p.Arg58Gln(p.R58Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96912489:96912489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669A>C
AA Mutation	p.Glu223Asp(p.E223D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97099733:97099733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2287G>A
AA Mutation	p.Glu763Lys(p.E763K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97247739:97247739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2744A>G
AA Mutation	p.Asn915Ser(p.N915S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97247788:97247788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2793G>T
AA Mutation	p.Lys931Asn(p.K931N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97348244:97348244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2973C>A
AA Mutation	p.Phe991Leu(p.F991L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96937330:96937330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187A>G
AA Mutation	p.Asn396Ser(p.N396S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96942083:96942083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391A>T
AA Mutation	p.Asp464Val(p.D464V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96738742:96738742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>C
AA Mutation	p.Asp108His(p.D108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96939275:96939275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218T>G
AA Mutation	p.Asn406Lys(p.N406K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96948957:96948957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201017046
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511Gln(p.R511Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96916544:96916544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839C>A
AA Mutation	p.Ser280Tyr(p.S280Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97072972:97072972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2082G>T
AA Mutation	p.Lys694Asn(p.K694N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96937339:96937339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41300144
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399Gln(p.R399Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96939319:96939319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262C>A
AA Mutation	p.Ala421Asp(p.A421D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96685089:96685089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	96957917:96957917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757187745
CDS Mutation	c.1704G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	96957986:96957986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1773A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	96945546:96945546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375900282
CDS Mutation	c.1464G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000324765
Start	96738592:96738592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Ter(p.R58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000324765
Start	96949004:96949004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1579G>T
AA Mutation	p.Glu527Ter(p.E527*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324765
Start	96912394:96912395(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.660dupA
AA Mutation	p.Gln221ThrfsTer6(p.Q221Tfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000324765
Start	96916576:96916576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000324765
Start	96735757:96735757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DIAPH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97348171:97348171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2900A>G
AA Mutation	p.Asn967Ser(p.N967S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97429689:97429689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3185C>T
AA Mutation	p.Ala1062Val(p.A1062V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	97247771:97247771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2776C>T
Mutation Classification	Silent
Feature Type	Transcript