Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KIF20B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737812:89737812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761389049
CDS Mutation	c.2971G>A
AA Mutation	p.Glu991Lys(p.E991K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89719675:89719675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1691A>C
AA Mutation	p.Asn564Thr(p.N564T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737488:89737488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2647A>C
AA Mutation	p.Asn883His(p.N883H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89774029:89774029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5444G>A
AA Mutation	p.Arg1815Gln(p.R1815Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89726303:89726303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012A>C
AA Mutation	p.Asn671Thr(p.N671T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89717697:89717697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149456198
CDS Mutation	c.1246G>A
AA Mutation	p.Val416Ile(p.V416I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89717467:89717467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>A
AA Mutation	p.Glu366Lys(p.E366K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737618:89737618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752730939
CDS Mutation	c.2777A>G
AA Mutation	p.Asn926Ser(p.N926S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737785:89737785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2944A>G
AA Mutation	p.Ile982Val(p.I982V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89715144:89715144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89738346:89738346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3505A>C
AA Mutation	p.Ile1169Leu(p.I1169L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89772776:89772776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5330A>G
AA Mutation	p.Lys1777Arg(p.K1777R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89718796:89718796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358T>C
AA Mutation	p.Ile453Thr(p.I453T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89726479:89726479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188G>A
AA Mutation	p.Glu730Lys(p.E730K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89739081:89739081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89737805:89737805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2964A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89751437:89751437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4188G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89724087:89724087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1846C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89737844:89737844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3003T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89738591:89738591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3750A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89716473:89716473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89758852:89758852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4654delA
AA Mutation	p.Arg1552GlyfsTer9(p.R1552Gfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89754649:89754649(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755841488
CDS Mutation	c.4485delT
AA Mutation	p.Phe1495LeufsTer10(p.F1495Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89724010:89724010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1775delA
AA Mutation	p.Lys592ArgfsTer4(p.K592Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89718764:89718764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1332delT
AA Mutation	p.Phe444LeufsTer9(p.F444Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89738058:89738058(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3223delA
AA Mutation	p.Ser1075ValfsTer18(p.S1075Vfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89774033:89774033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5452delA
AA Mutation	p.Thr1818GlnfsTer47(p.T1818Qfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89738478:89738478(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3641delA
AA Mutation	p.Asn1214ThrfsTer5(p.N1214Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000371728
Start	89729158:89729158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2302G>T
AA Mutation	p.Glu768Ter(p.E768*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000371728
Start	89738589:89738589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3748G>T
AA Mutation	p.Glu1250Ter(p.E1250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89718763:89718764(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1332dupT
AA Mutation	p.Asn445Ter(p.N445*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF20B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737616:89737616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2775G>T
AA Mutation	p.Lys925Asn(p.K925N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89738422:89738422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3581T>C
AA Mutation	p.Ile1194Thr(p.I1194T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89718817:89718817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1379A>G
AA Mutation	p.Tyr460Cys(p.Y460C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737762:89737762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2921G>A
AA Mutation	p.Ser974Asn(p.S974N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89758840:89758840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4638A>C
AA Mutation	p.Glu1546Asp(p.E1546D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737446:89737446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2605C>G
AA Mutation	p.Pro869Ala(p.P869A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89709179:89709179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737812:89737812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761389049
CDS Mutation	c.2971G>A
AA Mutation	p.Glu991Lys(p.E991K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371728
Start	89737969:89737969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3128G>A
AA Mutation	p.Arg1043Gln(p.R1043Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89737802:89737802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746154873
CDS Mutation	c.2961G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371728
Start	89719700:89719700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371728
Start	89754564:89754564(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4399delA
AA Mutation	p.Met1467Ter(p.M1467*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000371728
Start	89738217:89738217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3376G>T
AA Mutation	p.Glu1126Ter(p.E1126*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000371728
Start	89738520:89738520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3679G>T
AA Mutation	p.Glu1227Ter(p.E1227*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript