Colon Cancer: Gene >> RTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59726934:59726934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750C>A
AA Mutation	p.Leu584Ile(p.L584I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59746330:59746330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393T>G
AA Mutation	p.Asn131Lys(p.N131K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59745943:59745943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.780T>A
AA Mutation	p.Phe260Leu(p.F260L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59607343:59607343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1915C>T
AA Mutation	p.Arg639Cys(p.R639C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59746100:59746100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623A>G
AA Mutation	p.Gln208Arg(p.Q208R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59727293:59727293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391G>A
AA Mutation	p.Ser464Asn(p.S464N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59727144:59727144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759537844
CDS Mutation	c.1540C>T
AA Mutation	p.Arg514Trp(p.R514W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59727509:59727509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772853362
CDS Mutation	c.1175C>T
AA Mutation	p.Pro392Leu(p.P392L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59745866:59745866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377312291
CDS Mutation	c.857C>T
AA Mutation	p.Thr286Met(p.T286M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59745791:59745791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932G>C
AA Mutation	p.Ser311Thr(p.S311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59607472:59607472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745946902
CDS Mutation	c.1786C>T
AA Mutation	p.Arg596Trp(p.R596W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59607448:59607448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756386522
CDS Mutation	c.1810G>A
AA Mutation	p.Val604Met(p.V604M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59727236:59727236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483Gln(p.R483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59607400:59607400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143124571
CDS Mutation	c.1858G>A
AA Mutation	p.Val620Met(p.V620M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59727164:59727164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1520A>G
AA Mutation	p.Glu507Gly(p.E507G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59607388:59607388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774462442
CDS Mutation	c.1870G>A
AA Mutation	p.Val624Met(p.V624M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59726956:59726956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768308668
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59727166:59727166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577451964
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59745748:59745748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59727127:59727127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763202784
CDS Mutation	c.1557G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59746180:59746180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59607305:59607305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11559110
CDS Mutation	c.1953C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267484
Start	59745978:59745978(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.745delA
AA Mutation	p.Ile249SerfsTer16(p.I249Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267484
Start	59745820:59745821(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.902_903insA
AA Mutation	p.Glu302Ter(p.E302*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59727584:59727584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535179762
CDS Mutation	c.1100C>T
AA Mutation	p.Ser367Leu(p.S367L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59745957:59745957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>C
AA Mutation	p.Glu256Gln(p.E256Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59746062:59746062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661G>A
AA Mutation	p.Asp221Asn(p.D221N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59746083:59746083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370975029
CDS Mutation	c.640G>A
AA Mutation	p.Glu214Lys(p.E214K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59746159:59746159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564G>C
AA Mutation	p.Gln188His(p.Q188H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267484
Start	59746160:59746160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563A>C
AA Mutation	p.Gln188Pro(p.Q188P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267484
Start	59603886:59603886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559148180
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript