Colon Cancer: Gene >> MYO1E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59218040:59218040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.958A>G
AA Mutation	p.Lys320Glu(p.K320E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59161097:59161097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778885841
CDS Mutation	c.2761G>A
AA Mutation	p.Gly921Arg(p.G921R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59231728:59231728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770956809
CDS Mutation	c.484G>A
AA Mutation	p.Val162Ile(p.V162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59208724:59208724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487A>G
AA Mutation	p.Asn496Ser(p.N496S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59208815:59208815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396G>T
AA Mutation	p.Val466Leu(p.V466L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59227550:59227550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551C>G
AA Mutation	p.Pro184Arg(p.P184R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59163255:59163255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529T>A
AA Mutation	p.Ser843Arg(p.S843R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59224747:59224747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719T>G
AA Mutation	p.Leu240Arg(p.L240R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59178404:59178404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2038G>A
AA Mutation	p.Ala680Thr(p.A680T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59217914:59217914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752138428
CDS Mutation	c.1084C>T
AA Mutation	p.Arg362Trp(p.R362W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59227502:59227502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599T>A
AA Mutation	p.Val200Glu(p.V200E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59272386:59272386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>A
AA Mutation	p.Asp23Asn(p.D23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59217944:59217944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054C>T
AA Mutation	p.Arg352Trp(p.R352W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59174191:59174191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757483863
CDS Mutation	c.2099G>A
AA Mutation	p.Arg700Gln(p.R700Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59153709:59153709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2961C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59208816:59208816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759846809
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59231759:59231759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531976863
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59224716:59224716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201439341
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59217960:59217960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59178480:59178480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770645366
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYO1E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59171933:59171933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2444A>T
AA Mutation	p.Lys815Ile(p.K815I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59188200:59188200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1822G>A
AA Mutation	p.Glu608Lys(p.E608K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288235
Start	59195495:59195495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11539755
CDS Mutation	c.1771G>A
AA Mutation	p.Glu591Lys(p.E591K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288235
Start	59205453:59205453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000288235
Start	59218037:59218037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>T
AA Mutation	p.Glu321Ter(p.E321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript