Colon Cancer: Gene >> NOX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155407192:155407192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518G>T
AA Mutation	p.Lys506Asn(p.K506N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155396954:155396954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589T>C
AA Mutation	p.Ile530Thr(p.I530T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155443313:155443313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>A
AA Mutation	p.Pro149His(p.P149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155436447:155436447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140761547
CDS Mutation	c.769G>A
AA Mutation	p.Val257Met(p.V257M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155443403:155443403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150612632
CDS Mutation	c.356C>T
AA Mutation	p.Ala119Val(p.A119V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155455065:155455065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113A>C
AA Mutation	p.Glu38Ala(p.E38A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155440101:155440101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773010080
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155396946:155396946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597T>C
AA Mutation	p.Phe533Leu(p.F533L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155455106:155455106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72T>G
AA Mutation	p.Phe24Leu(p.F24L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159060
Start	155443408:155443408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159060
Start	155443351:155443351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159060
Start	155422790:155422790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769487012
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159060
Start	155428985:155428985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761321329
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159060
Start	155436460:155436460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000159060
Start	155428906:155428906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1033delC
AA Mutation	p.Gln345ArgfsTer49(p.Q345Rfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000159060
Start	155428893:155428893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1046delT
AA Mutation	p.Phe349SerfsTer45(p.F349Sfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000159060
Start	155436438:155436439(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.777_778insG
AA Mutation	p.Phe260ValfsTer22(p.F260Vfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NOX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155430921:155430921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813T>G
AA Mutation	p.Ile271Met(p.I271M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155428944:155428944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376763861
CDS Mutation	c.995C>T
AA Mutation	p.Ser332Leu(p.S332L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000159060
Start	155454845:155454845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757425327
CDS Mutation	c.221G>A
AA Mutation	p.Arg74Gln(p.R74Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript