Colon Cancer: Gene >> SEMA4F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74673546:74673546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375899286
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Trp(p.R214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357877
Start	74662825:74662825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550G>A
AA Mutation	p.Gly184Arg(p.G184R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74674895:74674895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146041751
CDS Mutation	c.1009G>A
AA Mutation	p.Ala337Thr(p.A337T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74673794:74673794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747881367
CDS Mutation	c.788G>A
AA Mutation	p.Arg263His(p.R263H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74679943:74679943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775752097
CDS Mutation	c.2047C>T
AA Mutation	p.Arg683Cys(p.R683C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74680070:74680070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373277680
CDS Mutation	c.2174G>A
AA Mutation	p.Arg725Gln(p.R725Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74656560:74656560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746352642
CDS Mutation	c.172G>A
AA Mutation	p.Ala58Thr(p.A58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74679959:74679959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2063G>A
AA Mutation	p.Arg688Gln(p.R688Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357877
Start	74674542:74674542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183059394
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357877
Start	74673789:74673789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146708517
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357877
Start	74657882:74657882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357877
Start	74675201:74675202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1195_1196delTC
AA Mutation	p.Ser399ProfsTer3(p.S399Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357877
Start	74679719:74679719(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1828delC
AA Mutation	p.Arg610GlyfsTer9(p.R610Gfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000357877
Start	74679844:74679844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142022737
CDS Mutation	c.1948C>T
AA Mutation	p.Arg650Ter(p.R650*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357877
Start	74673455:74673456(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749720924
CDS Mutation	c.556dupG
AA Mutation	p.Val186GlyfsTer56(p.X186_splice)
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357877
Start	74675635:74675635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566725824
CDS Mutation	c.1482+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA4F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74656590:74656590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>A
AA Mutation	p.Leu68Ile(p.L68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74673742:74673742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765293054
CDS Mutation	c.736G>A
AA Mutation	p.Glu246Lys(p.E246K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357877
Start	74674667:74674667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992C>A
AA Mutation	p.Ser331Tyr(p.S331Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357877
Start	74673456:74673456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript