Colon Cancer: Gene >> NCAPD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134202875:134202875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548599881
CDS Mutation	c.1556G>A
AA Mutation	p.Arg519His(p.R519H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134168087:134168087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3482C>T
AA Mutation	p.Ser1161Phe(p.S1161F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134168540:134168540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3302A>C
AA Mutation	p.Lys1101Thr(p.K1101T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134220589:134220589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Glu68Lys(p.E68K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134177367:134177367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753417052
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958His(p.R958H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134153309:134153309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4307G>A
AA Mutation	p.Arg1436Gln(p.R1436Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134152969:134152969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4472A>C
AA Mutation	p.Lys1491Thr(p.K1491T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134194125:134194125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715G>A
AA Mutation	p.Cys572Tyr(p.C572Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134161821:134161821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3644A>G
AA Mutation	p.Asn1215Ser(p.N1215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134184651:134184651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781574921
CDS Mutation	c.2437C>T
AA Mutation	p.Pro813Ser(p.P813S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134206709:134206709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906A>C
AA Mutation	p.Gln302His(p.Q302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134210337:134210337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>C
AA Mutation	p.Lys167Thr(p.K167T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134160036:134160036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3723C>A
AA Mutation	p.Phe1241Leu(p.F1241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134184746:134184746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2342T>G
AA Mutation	p.Val781Gly(p.V781G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134204913:134204913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>T
AA Mutation	p.His359Tyr(p.H359Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134157068:134157068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4202C>T
AA Mutation	p.Ser1401Leu(p.S1401L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134168030:134168030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3539T>C
AA Mutation	p.Val1180Ala(p.V1180A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134177377:134177377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765167360
CDS Mutation	c.2863G>A
AA Mutation	p.Val955Met(p.V955M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134178915:134178915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2581G>T
AA Mutation	p.Gly861Trp(p.G861W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534548
Start	134158367:134158367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3996T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534548
Start	134204076:134204076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534548
Start	134169051:134169051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765047707
CDS Mutation	c.3105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534548
Start	134206654:134206654(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.961delC
AA Mutation	p.Ala322LeufsTer24(p.A322Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534548
Start	134178691:134178691(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2725delC
AA Mutation	p.Gln909ArgfsTer10(p.Q909Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534548
Start	134178690:134178691(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs770284236
CDS Mutation	c.2725dupC
AA Mutation	p.Gln909ProfsTer12(p.Q909Pfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534548
Start	134168141:134168142(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3427dupT
AA Mutation	p.Ser1143PhefsTer5(p.S1143Ffs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000534548
Start	134184753:134184753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000534548
Start	134209380:134209381(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.664_665insGGCCTG
AA Mutation	p.Asn222delinsArgProAsp(p.N222delinsRPD)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NCAPD3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000534548
Start	134184903:134184903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2335G>C
AA Mutation	p.Asp779His(p.D779H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000534548
Start	134203153:134203153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514G>T
AA Mutation	p.Arg505Ile(p.R505I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript