Colon Cancer: Gene >> MYO1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1471109:1471109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2174C>T
AA Mutation	p.Ala725Val(p.A725V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1472130:1472130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1896A>T
AA Mutation	p.Lys632Asn(p.K632N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1470263:1470263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377675305
CDS Mutation	c.2438G>A
AA Mutation	p.Arg813His(p.R813H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1480827:1480827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686A>G
AA Mutation	p.His229Arg(p.H229R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1483052:1483052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540764663
CDS Mutation	c.355G>A
AA Mutation	p.Val119Met(p.V119M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1470270:1470270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2431C>A
AA Mutation	p.His811Asn(p.H811N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1474680:1474680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727G>A
AA Mutation	p.Ser576Asn(p.S576N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1467486:1467486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3059A>G
AA Mutation	p.Gln1020Arg(p.Q1020R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1469560:1469560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368905625
CDS Mutation	c.2581C>T
AA Mutation	p.Arg861Trp(p.R861W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1479606:1479606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1006A>G
AA Mutation	p.Lys336Glu(p.K336E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1479650:1479650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962C>T
AA Mutation	p.Ala321Val(p.A321V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1465730:1465730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3188G>T
AA Mutation	p.Arg1063Leu(p.R1063L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1482911:1482911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769587880
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359786
Start	1471935:1471935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770632413
CDS Mutation	c.1993C>T
AA Mutation	p.Arg665Cys(p.R665C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359786
Start	1478685:1478685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767932819
CDS Mutation	c.1143C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359786
Start	1482505:1482505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359786
Start	1478703:1478703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150488154
CDS Mutation	c.1125G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359786
Start	1480877:1480877(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.636delC
AA Mutation	p.Val213TrpfsTer56(p.V213Wfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000359786
Start	1471263:1471263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140238692
CDS Mutation	c.2095C>T
AA Mutation	p.Arg699Ter(p.R699*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MYO1C

No Mutation Annotation!