Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SETD1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121810450:121810450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505G>A
AA Mutation	p.Arg502His(p.R502H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121817805:121817805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3319G>A
AA Mutation	p.Asp1107Asn(p.D1107N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121806022:121806022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461T>C
AA Mutation	p.Val154Ala(p.V154A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121814743:121814743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2528C>T
AA Mutation	p.Ser843Leu(p.S843L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121823525:121823525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188682228
CDS Mutation	c.4946G>A
AA Mutation	p.Arg1649His(p.R1649H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121827939:121827939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5596G>A
AA Mutation	p.Ala1866Thr(p.A1866T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121830124:121830124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5786C>T
AA Mutation	p.Ser1929Leu(p.S1929L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121823207:121823207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4628C>G
AA Mutation	p.Ala1543Gly(p.A1543G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121817466:121817466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199987652
CDS Mutation	c.3074G>A
AA Mutation	p.Arg1025Gln(p.R1025Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121827828:121827828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5563G>A
AA Mutation	p.Glu1855Lys(p.E1855K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121814575:121814575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764972287
CDS Mutation	c.2360C>T
AA Mutation	p.Thr787Met(p.T787M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121823498:121823498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4919G>T
AA Mutation	p.Gly1640Val(p.G1640V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121810027:121810027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082G>C
AA Mutation	p.Gly361Ala(p.G361A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121822589:121822589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760562324
CDS Mutation	c.4010C>T
AA Mutation	p.Pro1337Leu(p.P1337L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121830156:121830156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5818A>G
AA Mutation	p.Thr1940Ala(p.T1940A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121810071:121810071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126G>A
AA Mutation	p.Ala376Thr(p.A376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121814442:121814442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2227C>T
AA Mutation	p.Pro743Ser(p.P743S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121814254:121814254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2039C>T
AA Mutation	p.Pro680Leu(p.P680L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121814195:121814195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980G>A
AA Mutation	p.Met660Ile(p.M660I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121819775:121819775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3790G>A
AA Mutation	p.Asp1264Asn(p.D1264N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121810510:121810510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1565C>T
AA Mutation	p.Ser522Leu(p.S522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121819629:121819629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3644A>G
AA Mutation	p.Glu1215Gly(p.E1215G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121823711:121823711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5132T>G
AA Mutation	p.Met1711Arg(p.M1711R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121804757:121804757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20C>A
AA Mutation	p.Pro7His(p.P7H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121817620:121817620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3228G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121814612:121814612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2397C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121814648:121814648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2433T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121822788:121822788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4209G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121810478:121810478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121819738:121819738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121809767:121809767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121827791:121827791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777144386
CDS Mutation	c.5526C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121822989:121822989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121828043:121828043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375243812
CDS Mutation	c.5700C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121810214:121810214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121814414:121814414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763944606
CDS Mutation	c.2199G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121809902:121809902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543855650
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000604567
Start	121810082:121810082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121804752:121804752(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.22delC
AA Mutation	p.His8ThrfsTer27(p.H8Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121819645:121819645(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3664delG
AA Mutation	p.Ala1222HisfsTer53(p.A1222Hfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121823338:121823338(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4765delC
AA Mutation	p.Gln1589SerfsTer11(p.Q1589Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121810620:121810620(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1680delC
AA Mutation	p.Ser561ArgfsTer47(p.S561Rfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121805178:121805178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.239delA
AA Mutation	p.Asn80ThrfsTer26(p.N80Tfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121823172:121823173(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4595dupT
AA Mutation	p.Leu1532PhefsTer35(p.L1532Ffs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SETD1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121823560:121823560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372037884
CDS Mutation	c.4981G>A
AA Mutation	p.Glu1661Lys(p.E1661K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000604567
Start	121819439:121819439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3454G>A
AA Mutation	p.Ala1152Thr(p.A1152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000604567
Start	121804752:121804752(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.22delC
AA Mutation	p.His8ThrfsTer27(p.H8Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript