Colon Cancer: Gene >> NPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153689283:153689283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758216180
CDS Mutation	c.2660C>T
AA Mutation	p.Ala887Val(p.A887V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153681711:153681711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043C>A
AA Mutation	p.Thr348Asn(p.T348N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153689234:153689234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2611G>A
AA Mutation	p.Ala871Thr(p.A871T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153689957:153689957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144189754
CDS Mutation	c.2909G>A
AA Mutation	p.Arg970His(p.R970H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153683428:153683428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737934
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439His(p.R439H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153689211:153689211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763954604
CDS Mutation	c.2588G>A
AA Mutation	p.Arg863His(p.R863H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153687684:153687684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770463801
CDS Mutation	c.2143C>T
AA Mutation	p.Arg715Trp(p.R715W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153680686:153680686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>T
AA Mutation	p.Arg303Cys(p.R303C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153688196:153688196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753081607
CDS Mutation	c.2392C>T
AA Mutation	p.Arg798Cys(p.R798C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368680
Start	153689007:153689007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372297612
CDS Mutation	c.2472G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368680
Start	153683462:153683462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368680
Start	153681827:153681827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368680
Start	153686699:153686699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1818delC
AA Mutation	p.Asn607IlefsTer62(p.N607Ifs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368680
Start	153688085:153688085(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2286delC
AA Mutation	p.Phe763SerfsTer37(p.F763Sfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000368680
Start	153684995:153684995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1516G>T
AA Mutation	p.Glu506Ter(p.E506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153688196:153688196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753081607
CDS Mutation	c.2392C>T
AA Mutation	p.Arg798Cys(p.R798C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153689933:153689933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199989132
CDS Mutation	c.2885G>A
AA Mutation	p.Arg962His(p.R962H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153685011:153685011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532G>T
AA Mutation	p.Arg511Leu(p.R511L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368680
Start	153685023:153685023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544T>G
AA Mutation	p.Val515Gly(p.V515G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368680
Start	153685081:153685081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554024271
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript