Colon Cancer: Gene >> XPO5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43573573:43573573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134C>A
AA Mutation	p.Pro45His(p.P45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43548331:43548331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759225284
CDS Mutation	c.1990C>T
AA Mutation	p.Arg664Cys(p.R664C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43560955:43560955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064C>A
AA Mutation	p.Ser355Tyr(p.S355Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43547612:43547612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2156C>T
AA Mutation	p.Ala719Val(p.A719V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265351
Start	43546751:43546751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2162T>C
AA Mutation	p.Met721Thr(p.M721T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265351
Start	43560178:43560178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221G>T
AA Mutation	p.Lys407Asn(p.K407N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43572573:43572573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746237786
CDS Mutation	c.233G>A
AA Mutation	p.Arg78Gln(p.R78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43558587:43558587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Gly409Asp(p.G409D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43531525:43531525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377196219
CDS Mutation	c.2494G>A
AA Mutation	p.Val832Ile(p.V832I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43558508:43558508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305C>A
AA Mutation	p.Phe435Leu(p.F435L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43560204:43560204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Cys(p.R399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43523902:43523902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3581A>G
AA Mutation	p.Asp1194Gly(p.D1194G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265351
Start	43548322:43548322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760578587
CDS Mutation	c.1999G>A
AA Mutation	p.Val667Met(p.V667M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265351
Start	43562274:43562274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754664679
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265351
Start	43534004:43534004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2346C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265351
Start	43570914:43570914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265351
Start	43553445:43553445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772506045
CDS Mutation	c.1500C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265351
Start	43547686:43547686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2082T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265351
Start	43560271:43560272(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1127dupG
AA Mutation	p.Ala377SerfsTer6(p.A377Sfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> XPO5

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265351
Start	43524634:43524634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3314G>A
AA Mutation	p.Arg1105His(p.R1105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265351
Start	43548326:43548326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1995G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000265351
Start	43553390:43553390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555C>T
AA Mutation	p.Arg519Ter(p.R519*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript