Colon Cancer: Gene >> MYO1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191364224:191364224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762103792
CDS Mutation	c.980G>A
AA Mutation	p.Arg327Gln(p.R327Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191364209:191364209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749571664
CDS Mutation	c.965G>A
AA Mutation	p.Arg322Gln(p.R322Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191370288:191370288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181T>C
AA Mutation	p.Phe394Ser(p.F394S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191385953:191385953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423T>G
AA Mutation	p.Phe475Val(p.F475V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191396472:191396472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2270T>G
AA Mutation	p.Ile757Ser(p.I757S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191416224:191416224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769052951
CDS Mutation	c.3269A>G
AA Mutation	p.Asn1090Ser(p.N1090S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191390399:191390399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889C>T
AA Mutation	p.Ala630Val(p.A630V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191329949:191329949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266A>G
AA Mutation	p.Asp89Gly(p.D89G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191392177:191392177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052G>T
AA Mutation	p.Lys684Asn(p.K684N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191408134:191408134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2576A>G
AA Mutation	p.Lys859Arg(p.K859R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191341562:191341562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448G>A
AA Mutation	p.Glu150Lys(p.E150K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191393089:191393089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2093A>G
AA Mutation	p.Asp698Gly(p.D698G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304164
Start	191381500:191381500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147109563
CDS Mutation	c.1224C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304164
Start	191364168:191364168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304164
Start	191277003:191277003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304164
Start	191393178:191393178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2188delA
AA Mutation	p.Ser730AlafsTer4(p.S730Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000304164
Start	191392187:191392187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2062C>T
AA Mutation	p.Arg688Ter(p.R688*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000304164
Start	191369608:191369608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Ter(p.R367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304164
Start	191390310:191390311(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1806dupA
AA Mutation	p.Ala603SerfsTer37(p.A603Sfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304164
Start	191411140:191411141(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2842_2843insGT
AA Mutation	p.Phe948CysfsTer47(p.F948Cfs*47)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYO1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191408185:191408185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2627G>T
AA Mutation	p.Arg876Ile(p.R876I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191416145:191416145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3190C>A
AA Mutation	p.Leu1064Ile(p.L1064I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191350186:191350186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>T
AA Mutation	p.Asp175Tyr(p.D175Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304164
Start	191393172:191393172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2176C>A
AA Mutation	p.Leu726Ile(p.L726I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304164
Start	191296125:191296125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000304164
Start	191369608:191369608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Ter(p.R367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000304164
Start	191363833:191363833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Ter(p.R291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000304164
Start	191400385:191400385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2299C>T
AA Mutation	p.Arg767Ter(p.R767*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript