Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRDM16

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000270722
Start	3426224:3426224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201439415
CDS Mutation	c.3283C>T
AA Mutation	p.Arg1095Trp(p.R1095W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3430935:3430935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3348G>T
AA Mutation	p.Glu1116Asp(p.E1116D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3402823:3402823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764674939
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411568:3411568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1371T>G
AA Mutation	p.Phe457Leu(p.F457L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3414628:3414628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573567598
CDS Mutation	c.2672C>T
AA Mutation	p.Pro891Leu(p.P891L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3432051:3432051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3607G>A
AA Mutation	p.Glu1203Lys(p.E1203K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3405531:3405531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774523031
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Cys(p.R357C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3432040:3432040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772196588
CDS Mutation	c.3596G>A
AA Mutation	p.Arg1199His(p.R1199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3404861:3404861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007G>A
AA Mutation	p.Arg336His(p.R336H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3186157:3186157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>T
AA Mutation	p.Pro24Ser(p.P24S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3433714:3433714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3734C>A
AA Mutation	p.Pro1245His(p.P1245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411581:3411581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384C>T
AA Mutation	p.Pro462Ser(p.P462S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412316:3412316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767432596
CDS Mutation	c.2119G>A
AA Mutation	p.Gly707Ser(p.G707S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412226:3412226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2029C>T
AA Mutation	p.Pro677Ser(p.P677S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412335:3412335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2138A>G
AA Mutation	p.Glu713Gly(p.E713G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411408:3411408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211C>T
AA Mutation	p.Thr404Met(p.T404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412049:3412049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852A>G
AA Mutation	p.Thr618Ala(p.T618A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3425597:3425597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2956C>T
AA Mutation	p.Arg986Cys(p.R986C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3432033:3432033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3589G>A
AA Mutation	p.Asp1197Asn(p.D1197N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3402982:3402982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868T>C
AA Mutation	p.Phe290Leu(p.F290L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3404866:3404866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012G>A
AA Mutation	p.Glu338Lys(p.E338K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3432078:3432078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3634C>T
AA Mutation	p.Leu1212Phe(p.L1212F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412127:3412127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61756438
CDS Mutation	c.1930G>A
AA Mutation	p.Glu644Lys(p.E644K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3404860:3404860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748880850
CDS Mutation	c.1006C>T
AA Mutation	p.Arg336Cys(p.R336C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412752:3412752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771456448
CDS Mutation	c.2555C>T
AA Mutation	p.Pro852Leu(p.P852L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3433684:3433684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3704C>T
AA Mutation	p.Ala1235Val(p.A1235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3404865:3404865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774182702
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3412093:3412093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1896C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3186306:3186306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3411877:3411877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565375368
CDS Mutation	c.1680C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3411445:3411445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747141437
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3426151:3426151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3430956:3430956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370420046
CDS Mutation	c.3369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3412081:3412081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762491643
CDS Mutation	c.1884C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3412531:3412531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2334G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3411430:3411430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1233G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270722
Start	3411729:3411729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1536delC
AA Mutation	p.Gly513AlafsTer27(p.G513Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000270722
Start	3417984:3417984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2848C>T
AA Mutation	p.Arg950Ter(p.R950*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270722
Start	3411849:3411850(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1656dupG
AA Mutation	p.Asn553GlufsTer51(p.N553Efs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PRDM16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3385201:3385201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201182055
CDS Mutation	c.488C>T
AA Mutation	p.Ala163Val(p.A163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412070:3412070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1873C>A
AA Mutation	p.Leu625Met(p.L625M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3405542:3405542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761160322
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3411934:3411934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35579804
CDS Mutation	c.1737C>T
Mutation Classification	Silent
Feature Type	Transcript