Colon Cancer: Gene >> NOS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151013339:151013339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3215G>A
AA Mutation	p.Arg1072Gln(p.R1072Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151014026:151014026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3469G>A
AA Mutation	p.Glu1157Lys(p.E1157K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151013847:151013847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3379G>A
AA Mutation	p.Val1127Met(p.V1127M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151010902:151010902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2900G>A
AA Mutation	p.Gly967Glu(p.G967E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151009420:151009420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2347C>A
AA Mutation	p.Leu783Met(p.L783M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	150998612:150998612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368296624
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151001573:151001573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458G>T
AA Mutation	p.Lys486Asn(p.K486N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	150998982:150998982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853C>G
AA Mutation	p.Arg285Gly(p.R285G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	150998399:150998399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625A>G
AA Mutation	p.Thr209Ala(p.T209A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151009538:151009538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762247400
CDS Mutation	c.2465C>T
AA Mutation	p.Ala822Val(p.A822V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151010138:151010138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2536C>T
AA Mutation	p.Arg846Trp(p.R846W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151013317:151013317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3193C>A
AA Mutation	p.Gln1065Lys(p.Q1065K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151013790:151013790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757784663
CDS Mutation	c.3322C>T
AA Mutation	p.Arg1108Trp(p.R1108W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151010667:151010667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370602493
CDS Mutation	c.2756C>T
AA Mutation	p.Pro919Leu(p.P919L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151010277:151010277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2675C>T
AA Mutation	p.Ala892Val(p.A892V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151001409:151001409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774225083
CDS Mutation	c.1412C>T
AA Mutation	p.Pro471Leu(p.P471L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151010201:151010201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762840310
CDS Mutation	c.2599T>A
AA Mutation	p.Ser867Thr(p.S867T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000297494
Start	151007104:151007104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1940T>G
AA Mutation	p.Phe647Cys(p.F647C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	150995308:150995308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757296609
CDS Mutation	c.264G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151013262:151013262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756428247
CDS Mutation	c.3138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151001552:151001552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151013774:151013774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151001896:151001896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751070801
CDS Mutation	c.1578C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151013786:151013786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200424809
CDS Mutation	c.3318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	150998617:150998617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567077361
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151007129:151007129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1965G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	151007105:151007105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1941C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297494
Start	150998560:150998560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759150325
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297494
Start	151001310:151001310(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1319delG
AA Mutation	p.Gly440AlafsTer64(p.G440Afs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297494
Start	151006986:151006986(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1921delG
AA Mutation	p.Ala641ProfsTer97(p.A641Pfs*97)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297494
Start	151010123:151010123(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2526delC
AA Mutation	p.Gly843AlafsTer115(p.G843Afs*115)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NOS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	150999219:150999219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>A
AA Mutation	p.Arg329His(p.R329H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297494
Start	151001550:151001550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>A
AA Mutation	p.Pro479Thr(p.P479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript