Colon Cancer: Gene >> DNM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10802291:10802291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426C>A
AA Mutation	p.Leu476Ile(p.L476I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10786600:10786600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886C>A
AA Mutation	p.Leu296Ile(p.L296I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10796119:10796119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255A>C
AA Mutation	p.Lys419Gln(p.K419Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10829133:10829133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2156G>A
AA Mutation	p.Arg719Gln(p.R719Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10829147:10829147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749953105
CDS Mutation	c.2170C>T
AA Mutation	p.Arg724Cys(p.R724C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10775772:10775772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455T>C
AA Mutation	p.Ile152Thr(p.I152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10812349:10812349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1643A>G
AA Mutation	p.Glu548Gly(p.E548G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10777171:10777171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145478270
CDS Mutation	c.643G>A
AA Mutation	p.Asp215Asn(p.D215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355667
Start	10829254:10829254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757565933
CDS Mutation	c.2277C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355667
Start	10830226:10830226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777834732
CDS Mutation	c.2391C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355667
Start	10782967:10782967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355667
Start	10829098:10829098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2121C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355667
Start	10830206:10830206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2377delC
AA Mutation	p.Leu793Ter(p.L793*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000355667
Start	10718360:10718360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.118C>T
AA Mutation	p.Gln40Ter(p.Q40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355667
Start	10830205:10830206(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764391392
CDS Mutation	c.2377dupC
AA Mutation	p.Leu793ProfsTer31(p.L793Pfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000355667
Start	10825089:10825091(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1928_1930delTCT
AA Mutation	p.Phe643del(p.F643del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DNM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10796095:10796095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231G>C
AA Mutation	p.Ala411Pro(p.A411P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10777166:10777166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>A
AA Mutation	p.Gly213Asp(p.G213D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10796078:10796078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214C>T
AA Mutation	p.Pro405Leu(p.P405L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10793817:10793817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Cys(p.R364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10796092:10796092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228G>A
AA Mutation	p.Glu410Lys(p.E410K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10825075:10825075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587778236
CDS Mutation	c.1912G>A
AA Mutation	p.Ala638Thr(p.A638T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10793809:10793809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082G>A
AA Mutation	p.Arg361Gln(p.R361Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355667
Start	10830173:10830173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2338C>T
AA Mutation	p.Arg780Trp(p.R780W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355667
Start	10759783:10759783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355667
Start	10829185:10829185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755163979
CDS Mutation	c.2208C>T
Mutation Classification	Silent
Feature Type	Transcript