Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NOS2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000313735
Start	27788930:27788930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197A>T
AA Mutation	p.Lys66Met(p.K66M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27774357:27774357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376C>G
AA Mutation	p.Ala459Gly(p.A459G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27778980:27778980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780524247
CDS Mutation	c.1081G>A
AA Mutation	p.Gly361Ser(p.G361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27781152:27781152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141690665
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Trp(p.R250W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27780869:27780869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200678947
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27766519:27766519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377596177
CDS Mutation	c.2237C>T
AA Mutation	p.Pro746Leu(p.P746L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27759005:27759005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3230G>A
AA Mutation	p.Gly1077Asp(p.G1077D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27764016:27764016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2314808
CDS Mutation	c.2557G>A
AA Mutation	p.Glu853Lys(p.E853K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27779007:27779007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>A
AA Mutation	p.Val352Met(p.V352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27761205:27761205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753799387
CDS Mutation	c.2827G>A
AA Mutation	p.Val943Ile(p.V943I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27772423:27772423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589G>A
AA Mutation	p.Arg530His(p.R530H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27787787:27787787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358A>C
AA Mutation	p.Met120Leu(p.M120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27782990:27782990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200238137
CDS Mutation	c.584G>A
AA Mutation	p.Arg195His(p.R195H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27769003:27769003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200815966
CDS Mutation	c.2008C>T
AA Mutation	p.Arg670Cys(p.R670C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27762879:27762879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2719T>C
AA Mutation	p.Phe907Leu(p.F907L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27757343:27757343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748134272
CDS Mutation	c.3365G>A
AA Mutation	p.Arg1122His(p.R1122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27762880:27762880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2718G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27789628:27789628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773527134
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27782101:27782101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776581126
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27779020:27779020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201471682
CDS Mutation	c.1041C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27772428:27772428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1584G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27773226:27773226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27769010:27769010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144098330
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313735
Start	27760672:27760672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201753717
CDS Mutation	c.2961G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313735
Start	27769063:27769063(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1948delG
AA Mutation	p.Ala650ProfsTer53(p.A650Pfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313735
Start	27767745:27767745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2127delC
AA Mutation	p.Tyr709Ter(p.Y709*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000313735
Start	27763984:27763984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2589C>A
AA Mutation	p.Cys863Ter(p.C863*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NOS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27757335:27757335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3373G>A
AA Mutation	p.Glu1125Lys(p.E1125K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27773200:27773200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1520G>T
AA Mutation	p.Arg507Ile(p.R507I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313735
Start	27782075:27782075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662G>A
AA Mutation	p.Arg221Gln(p.R221Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript