Colon Cancer: Gene >> MYT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64207641:64207641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546737046
CDS Mutation	c.445G>A
AA Mutation	p.Ala149Thr(p.A149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64232228:64232228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748649577
CDS Mutation	c.2740G>A
AA Mutation	p.Ala914Thr(p.A914T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64207689:64207689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761816010
CDS Mutation	c.493G>A
AA Mutation	p.Ala165Thr(p.A165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64207872:64207872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Glu226Lys(p.E226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64222043:64222043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2392C>T
AA Mutation	p.Leu798Phe(p.L798F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64232249:64232249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759011128
CDS Mutation	c.2761G>A
AA Mutation	p.Ala921Thr(p.A921T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64207884:64207884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146347952
CDS Mutation	c.688G>A
AA Mutation	p.Glu230Lys(p.E230K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64205717:64205717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751535010
CDS Mutation	c.314C>T
AA Mutation	p.Ser105Leu(p.S105L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64213559:64213559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766816369
CDS Mutation	c.1543G>A
AA Mutation	p.Ala515Thr(p.A515T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64217275:64217275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1840T>C
AA Mutation	p.Phe614Leu(p.F614L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64240375:64240375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781757453
CDS Mutation	c.3293A>G
AA Mutation	p.Tyr1098Cys(p.Y1098C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64208122:64208122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926C>T
AA Mutation	p.Pro309Leu(p.P309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64217228:64217228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598His(p.R598H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64208295:64208295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099T>C
AA Mutation	p.Ser367Pro(p.S367P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64219734:64219734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143909600
CDS Mutation	c.1993G>A
AA Mutation	p.Glu665Lys(p.E665K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64223320:64223320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2489G>A
AA Mutation	p.Ser830Asn(p.S830N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64236608:64236608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2951G>A
AA Mutation	p.Gly984Glu(p.G984E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64219866:64219866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2125G>A
AA Mutation	p.Ala709Thr(p.A709T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64218931:64218931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1867G>A
AA Mutation	p.Ala623Thr(p.A623T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64205760:64205760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375643178
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64208099:64208099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs797011037
CDS Mutation	c.903A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64208102:64208102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64232212:64232212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780216885
CDS Mutation	c.2724C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000328439
Start	64219776:64219776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2035C>T
AA Mutation	p.Arg679Ter(p.R679*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000328439
Start	64227463:64227463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2577C>A
AA Mutation	p.Tyr859Ter(p.Y859*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328439
Start	64205564:64205565(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.166dupC
AA Mutation	p.Leu56ProfsTer11(p.L56Pfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000328439
Start	64221892:64221892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2242-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MYT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64207872:64207872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Glu226Lys(p.E226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000328439
Start	64236646:64236646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2989G>T
AA Mutation	p.Val997Leu(p.V997L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64208078:64208078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882G>C
AA Mutation	p.Glu294Asp(p.E294D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64208096:64208096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900G>T
AA Mutation	p.Glu300Asp(p.E300D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64217257:64217257(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	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64240332:64240332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752441247
CDS Mutation	c.3250G>A
AA Mutation	p.Glu1084Lys(p.E1084K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64237354:64237354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765299378
CDS Mutation	c.3057G>A
Mutation Classification	Silent
Feature Type	Transcript