Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MYH7B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34997297:34997297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3530C>T
AA Mutation	p.Ala1177Val(p.A1177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	35000592:35000592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5207A>T
AA Mutation	p.Glu1736Val(p.E1736V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34990135:34990135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2015G>T
AA Mutation	p.Gly672Val(p.G672V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34978049:34978049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170G>A
AA Mutation	p.Arg57His(p.R57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34997269:34997269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3502G>A
AA Mutation	p.Glu1168Lys(p.E1168K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	35001293:35001293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758567295
CDS Mutation	c.5650G>A
AA Mutation	p.Glu1884Lys(p.E1884K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34988248:34988248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780052739
CDS Mutation	c.1699G>A
AA Mutation	p.Asp567Asn(p.D567N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34990097:34990097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1977G>T
AA Mutation	p.Gln659His(p.Q659H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34999169:34999169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4430T>C
AA Mutation	p.Val1477Ala(p.V1477A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34999252:34999252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771512439
CDS Mutation	c.4513C>T
AA Mutation	p.Arg1505Trp(p.R1505W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34998604:34998604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199900154
CDS Mutation	c.4094G>A
AA Mutation	p.Arg1365Gln(p.R1365Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34987780:34987780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1408G>T
AA Mutation	p.Gly470Trp(p.G470W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34997542:34997542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3775C>G
AA Mutation	p.Leu1259Val(p.L1259V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34980684:34980684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575C>T
AA Mutation	p.Pro192Leu(p.P192L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262873
Start	34985129:34985129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931T>C
AA Mutation	p.Tyr311His(p.Y311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34994160:34994160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770471792
CDS Mutation	c.2585C>T
AA Mutation	p.Thr862Ile(p.T862I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34987180:34987180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166A>G
AA Mutation	p.Asp389Gly(p.D389G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34994192:34994192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2617G>A
AA Mutation	p.Val873Ile(p.V873I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34998876:34998876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4277C>A
AA Mutation	p.Ala1426Glu(p.A1426E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34994197:34994197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2622G>T
AA Mutation	p.Lys874Asn(p.K874N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34977995:34977995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116G>A
AA Mutation	p.Ser39Asn(p.S39N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	35002071:35002071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771191903
CDS Mutation	c.5926G>A
AA Mutation	p.Ala1976Thr(p.A1976T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34996374:34996374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200331773
CDS Mutation	c.3098C>T
AA Mutation	p.Ala1033Val(p.A1033V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34999208:34999208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763069439
CDS Mutation	c.4469C>T
AA Mutation	p.Ala1490Val(p.A1490V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34997258:34997258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3491C>T
AA Mutation	p.Ala1164Val(p.A1164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262873
Start	34991121:34991121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769933919
CDS Mutation	c.2309G>A
AA Mutation	p.Arg770Gln(p.R770Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34979695:34979695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359T>C
AA Mutation	p.Met120Thr(p.M120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34979741:34979741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34979424:34979424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34979702:34979702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200343489
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34988241:34988241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756378962
CDS Mutation	c.1692T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34994350:34994350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749996697
CDS Mutation	c.2775G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34996502:34996502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3226C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34994248:34994248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191773517
CDS Mutation	c.2673G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34998393:34998393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367556657
CDS Mutation	c.3972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34995476:34995476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2967G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000262873
Start	34987840:34987840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468C>T
AA Mutation	p.Gln490Ter(p.Q490*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000262873
Start	34997151:34997153(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762269210
CDS Mutation	c.3467_3469delAGA
AA Mutation	p.Lys1156del(p.K1156del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000262873
Start	34996741:34996743(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762599007
CDS Mutation	c.3379_3381delGAG
AA Mutation	p.Glu1127del(p.E1127del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MYH7B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34999252:34999252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771512439
CDS Mutation	c.4513C>T
AA Mutation	p.Arg1505Trp(p.R1505W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34980609:34980609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>T
AA Mutation	p.Asn167Ile(p.N167I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34990282:34990282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754220790
CDS Mutation	c.2075C>T
AA Mutation	p.Ser692Leu(p.S692L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34985074:34985074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876C>A
AA Mutation	p.Phe292Leu(p.F292L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262873
Start	34990097:34990097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1977G>T
AA Mutation	p.Gln659His(p.Q659H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	35001307:35001307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5664C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262873
Start	34989895:34989895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369651613
CDS Mutation	c.1869C>T
Mutation Classification	Silent
Feature Type	Transcript