Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MYH14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50249018:50249018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337C>T
AA Mutation	p.Ala446Val(p.A446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50276813:50276813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3614G>A
AA Mutation	p.Arg1205His(p.R1205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50276001:50276001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775122875
CDS Mutation	c.3355G>A
AA Mutation	p.Glu1119Lys(p.E1119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50223302:50223302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745491664
CDS Mutation	c.646G>A
AA Mutation	p.Ala216Thr(p.A216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50286660:50286660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4595C>G
AA Mutation	p.Ala1532Gly(p.A1532G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50281796:50281796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776280390
CDS Mutation	c.4370G>A
AA Mutation	p.Arg1457Gln(p.R1457Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50252676:50252676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762536654
CDS Mutation	c.1844T>C
AA Mutation	p.Met615Thr(p.M615T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50272668:50272668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369620344
CDS Mutation	c.3281G>A
AA Mutation	p.Arg1094Gln(p.R1094Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50247073:50247073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419His(p.R419H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50261502:50261502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2329C>A
AA Mutation	p.Leu777Ile(p.L777I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50290962:50290962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556548077
CDS Mutation	c.4918G>A
AA Mutation	p.Glu1640Lys(p.E1640K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50276037:50276037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3391C>T
AA Mutation	p.Arg1131Trp(p.R1131W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50210576:50210576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747518990
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50223339:50223339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767742973
CDS Mutation	c.683C>T
AA Mutation	p.Pro228Leu(p.P228L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376970
Start	50293565:50293565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5224G>A
AA Mutation	p.Ala1742Thr(p.A1742T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50290930:50290930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759824498
CDS Mutation	c.4886G>A
AA Mutation	p.Arg1629His(p.R1629H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50250647:50250647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200843734
CDS Mutation	c.1765C>T
AA Mutation	p.Arg589Trp(p.R589W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50286644:50286644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559910733
CDS Mutation	c.4579C>T
AA Mutation	p.Arg1527Trp(p.R1527W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376970
Start	50272562:50272562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3175C>T
AA Mutation	p.Arg1059Cys(p.R1059C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50278231:50278231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201181045
CDS Mutation	c.3851G>A
AA Mutation	p.Arg1284Gln(p.R1284Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50261617:50261617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761967521
CDS Mutation	c.2444G>A
AA Mutation	p.Arg815Gln(p.R815Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50250635:50250635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1753C>T
AA Mutation	p.Pro585Ser(p.P585S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50249117:50249117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436T>C
AA Mutation	p.Ile479Thr(p.I479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50210525:50210525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50249102:50249102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1421T>C
AA Mutation	p.Leu474Pro(p.L474P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50309735:50309735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5933C>A
AA Mutation	p.Pro1978His(p.P1978H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50268254:50268254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757682381
CDS Mutation	c.2797C>T
AA Mutation	p.Arg933Cys(p.R933C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50301791:50301791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5477G>T
AA Mutation	p.Arg1826Leu(p.R1826L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50293664:50293664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376798395
CDS Mutation	c.5323C>T
AA Mutation	p.Arg1775Cys(p.R1775C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50266970:50266970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2665G>A
AA Mutation	p.Ala889Thr(p.A889T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50281697:50281697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4271G>A
AA Mutation	p.Arg1424His(p.R1424H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50293601:50293601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373716045
CDS Mutation	c.5260C>T
AA Mutation	p.Arg1754Cys(p.R1754C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50250634:50250634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1752G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50252695:50252695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374682911
CDS Mutation	c.1863C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50271965:50271965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50210560:50210560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750733905
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50268237:50268237(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2784delG
AA Mutation	p.Arg929GlyfsTer44(p.R929Gfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50250520:50250520(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1643delC
AA Mutation	p.Pro548LeufsTer25(p.P548Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50271483:50271483(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2989delA
AA Mutation	p.Met997Ter(p.M997*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50309646:50309646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5848delC
AA Mutation	p.Leu1950SerfsTer14(p.L1950Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000376970
Start	50252662:50252662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830G>A
AA Mutation	p.Trp610Ter(p.W610*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50250519:50250520(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1643dupC
AA Mutation	p.Gly549TrpfsTer8(p.G549Wfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYH14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50261536:50261536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779829368
CDS Mutation	c.2363G>A
AA Mutation	p.Arg788Gln(p.R788Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50231982:50231982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368124508
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50276772:50276772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3573G>A
Mutation Classification	Silent
Feature Type	Transcript