Colon Cancer: Gene >> SEMA3F

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000002829
Start	50186283:50186283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748G>A
AA Mutation	p.Arg583Gln(p.R583Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50187961:50187961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753830480
CDS Mutation	c.2204C>T
AA Mutation	p.Ala735Val(p.A735V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50174345:50174345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50184617:50184617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259C>A
AA Mutation	p.Ser420Tyr(p.S420Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50182329:50182329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689A>G
AA Mutation	p.Asp230Gly(p.D230G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50187775:50187775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377363752
CDS Mutation	c.2018G>A
AA Mutation	p.Arg673His(p.R673H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50173883:50173883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203G>A
AA Mutation	p.Arg68His(p.R68H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50174274:50174274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752415195
CDS Mutation	c.380G>A
AA Mutation	p.Arg127Gln(p.R127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50182664:50182664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Glu262Lys(p.E262K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50184725:50184725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148796473
CDS Mutation	c.1367G>A
AA Mutation	p.Arg456His(p.R456H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002829
Start	50187770:50187770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373344301
CDS Mutation	c.2013C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002829
Start	50185456:50185456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002829
Start	50175122:50175122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002829
Start	50186659:50186659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760533853
CDS Mutation	c.1860C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000002829
Start	50187762:50187762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005C>T
AA Mutation	p.Gln669Ter(p.Q669*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000002829
Start	50182708:50182710(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.835_837delTTC
AA Mutation	p.Phe279del(p.F279del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA3F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50159702:50159702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>A
AA Mutation	p.Pro27Gln(p.P27Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000002829
Start	50188092:50188092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773078256
CDS Mutation	c.2335C>T
AA Mutation	p.Arg779Trp(p.R779W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002829
Start	50184780:50184780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540596745
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript