Colon Cancer: Gene >> CRMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5861085:5861085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201508359
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5836793:5836793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082G>A
AA Mutation	p.Arg361Gln(p.R361Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5841392:5841392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5856185:5856185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777531665
CDS Mutation	c.436G>A
AA Mutation	p.Asp146Asn(p.D146N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5856179:5856179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442G>A
AA Mutation	p.Val148Ile(p.V148I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5856173:5856173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448G>A
AA Mutation	p.Glu150Lys(p.E150K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5861110:5861110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>A
AA Mutation	p.Gln77Lys(p.Q77K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5828602:5828602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348G>T
AA Mutation	p.Gly450Cys(p.G450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5861034:5861034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305C>T
AA Mutation	p.Thr102Met(p.T102M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5835989:5835989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752604466
CDS Mutation	c.1207G>A
AA Mutation	p.Val403Met(p.V403M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5849403:5849403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610T>A
AA Mutation	p.Leu204Met(p.L204M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5828593:5828593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768538875
CDS Mutation	c.1357G>A
AA Mutation	p.Val453Ile(p.V453I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5828628:5828628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Gly441Asp(p.G441D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397890
Start	5835916:5835916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758401728
CDS Mutation	c.1280C>T
AA Mutation	p.Ser427Leu(p.S427L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5839634:5839634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376257908
CDS Mutation	c.856G>A
AA Mutation	p.Asp286Asn(p.D286N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5861156:5861156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752770907
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5856249:5856249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139688791
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5828537:5828537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1413G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5861111:5861111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5828540:5828540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370052265
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5836768:5836768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779301264
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5861042:5861042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5866718:5866718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370684622
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5861138:5861138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145307270
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397890
Start	5821794:5821794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1685delC
AA Mutation	p.Pro562LeufsTer21(p.P562Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397890
Start	5839665:5839665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.825delT
AA Mutation	p.Phe275LeufsTer28(p.F275Lfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000397890
Start	5825493:5825493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1627+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CRMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5828539:5828539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762086490
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Trp(p.R471W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5861152:5861152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147608754
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Trp(p.R63W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5849406:5849406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607G>T
AA Mutation	p.Asp203Tyr(p.D203Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5825498:5825498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623A>C
AA Mutation	p.Leu541Phe(p.L541F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5825500:5825500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621T>A
AA Mutation	p.Leu541Ile(p.L541I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5828593:5828593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768538875
CDS Mutation	c.1357G>A
AA Mutation	p.Val453Ile(p.V453I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5836062:5836062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397890
Start	5821794:5821794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1685delC
AA Mutation	p.Pro562LeufsTer21(p.P562Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript