Colon Cancer: Gene >> XPO6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28156081:28156081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>A
AA Mutation	p.Asp364Asn(p.D364N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28175921:28175921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377255371
CDS Mutation	c.382G>A
AA Mutation	p.Asp128Asn(p.D128N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28125719:28125719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748737569
CDS Mutation	c.1736G>A
AA Mutation	p.Arg579Gln(p.R579Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28169829:28169829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486G>T
AA Mutation	p.Glu162Asp(p.E162D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28156224:28156224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947T>A
AA Mutation	p.Ile316Asn(p.I316N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28101649:28101649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3085G>A
AA Mutation	p.Val1029Met(p.V1029M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28111870:28111870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145368246
CDS Mutation	c.2288G>A
AA Mutation	p.Arg763His(p.R763H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28107640:28107640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2379A>C
AA Mutation	p.Glu793Asp(p.E793D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28169878:28169878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437G>T
AA Mutation	p.Gly146Val(p.G146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28177315:28177315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112T>G
AA Mutation	p.Phe38Val(p.F38V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28156513:28156513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658A>G
AA Mutation	p.Asn220Asp(p.N220D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28146128:28146128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300A>C
AA Mutation	p.Ser434Arg(p.S434R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304658
Start	28104657:28104657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2835G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304658
Start	28107580:28107580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11557750
CDS Mutation	c.2439G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304658
Start	28125745:28125745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1710C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304658
Start	28106490:28106490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2505T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304658
Start	28175913:28175913(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.390delT
AA Mutation	p.Phe130LeufsTer7(p.F130Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304658
Start	28098557:28098557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3359delC
AA Mutation	p.Pro1120LeufsTer4(p.P1120Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000304658
Start	28156219:28156219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Glu318Ter(p.E318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304658
Start	28175912:28175913(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.390dupT
AA Mutation	p.Thr131TyrfsTer2(p.T131Yfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> XPO6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28113010:28113010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2045T>C
AA Mutation	p.Val682Ala(p.V682A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28146137:28146137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1291A>C
AA Mutation	p.Lys431Gln(p.K431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304658
Start	28111987:28111987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2171G>A
AA Mutation	p.Arg724Gln(p.R724Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304658
Start	28101566:28101566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3168C>T
Mutation Classification	Silent
Feature Type	Transcript