Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SEC16A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136475733:136475733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181091537
CDS Mutation	c.1883G>A
AA Mutation	p.Arg628His(p.R628H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474641:136474641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2975G>A
AA Mutation	p.Gly992Glu(p.G992E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474777:136474777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2839G>A
AA Mutation	p.Ala947Thr(p.A947T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136443857:136443857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6971C>T
AA Mutation	p.Ala2324Val(p.A2324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136451362:136451362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6206A>G
AA Mutation	p.Asp2069Gly(p.D2069G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136467065:136467065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772546770
CDS Mutation	c.3821G>A
AA Mutation	p.Arg1274His(p.R1274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136453455:136453455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6132A>C
AA Mutation	p.Glu2044Asp(p.E2044D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136463562:136463562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4548G>T
AA Mutation	p.Gln1516His(p.Q1516H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136476604:136476604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374603480
CDS Mutation	c.1012G>A
AA Mutation	p.Ala338Thr(p.A338T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136463597:136463597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763211212
CDS Mutation	c.4513G>A
AA Mutation	p.Asp1505Asn(p.D1505N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136455745:136455745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5713C>T
AA Mutation	p.Pro1905Ser(p.P1905S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136451359:136451359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371962258
CDS Mutation	c.6209G>A
AA Mutation	p.Arg2070His(p.R2070H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136456100:136456100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138068163
CDS Mutation	c.5617G>A
AA Mutation	p.Ala1873Thr(p.A1873T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474759:136474759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763734645
CDS Mutation	c.2857G>A
AA Mutation	p.Gly953Arg(p.G953R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136457559:136457559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5435G>A
AA Mutation	p.Arg1812His(p.R1812H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136475725:136475725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891G>A
AA Mutation	p.Val631Met(p.V631M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136459197:136459197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5346G>T
AA Mutation	p.Arg1782Ser(p.R1782S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136476798:136476798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474506:136474506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3110T>C
AA Mutation	p.Leu1037Pro(p.L1037P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136451350:136451350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768367463
CDS Mutation	c.6218C>T
AA Mutation	p.Ser2073Leu(p.S2073L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136476082:136476082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1534A>G
AA Mutation	p.Thr512Ala(p.T512A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136466087:136466087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4178C>T
AA Mutation	p.Pro1393Leu(p.P1393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136457494:136457494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5500C>A
AA Mutation	p.Leu1834Met(p.L1834M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136459799:136459799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202232995
CDS Mutation	c.5149G>A
AA Mutation	p.Asp1717Asn(p.D1717N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136466292:136466292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537949436
CDS Mutation	c.4100G>A
AA Mutation	p.Arg1367His(p.R1367H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136476925:136476925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691C>A
AA Mutation	p.Pro231Thr(p.P231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474734:136474734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2882G>A
AA Mutation	p.Ser961Asn(p.S961N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136466418:136466418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759715457
CDS Mutation	c.3974C>T
AA Mutation	p.Thr1325Met(p.T1325M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136475066:136475066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750113232
CDS Mutation	c.2550G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136451298:136451298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6270A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136475588:136475588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2028C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136447883:136447883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136476947:136476947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136463058:136463058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4722C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136459839:136459839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180816729
CDS Mutation	c.5109G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136456092:136456092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374142697
CDS Mutation	c.5625G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313050
Start	136475826:136475826(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1790delC
AA Mutation	p.Pro597ArgfsTer18(p.P597Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313050
Start	136447664:136447664(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6464delC
AA Mutation	p.Pro2155HisfsTer25(p.P2155Hfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000313050
Start	136455751:136455751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5707C>T
AA Mutation	p.Gln1903Ter(p.Q1903*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313050
Start	136477039:136477040(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.576dupT
AA Mutation	p.Asp193Ter(p.D193*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SEC16A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136459804:136459804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5144A>T
AA Mutation	p.Asn1715Ile(p.N1715I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136477585:136477585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>T
AA Mutation	p.Gly11Cys(p.G11C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136466432:136466432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368962662
CDS Mutation	c.3960C>T
Mutation Classification	Silent
Feature Type	Transcript