Colon Cancer: Gene >> SEMA4G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100979108:100979108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>A
AA Mutation	p.Leu274Met(p.L274M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100980140:100980140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761554973
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Cys(p.R383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100983785:100983785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777161655
CDS Mutation	c.2171C>T
AA Mutation	p.Ala724Val(p.A724V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100980584:100980584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754532026
CDS Mutation	c.1358G>A
AA Mutation	p.Gly453Asp(p.G453D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100983652:100983652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2038G>A
AA Mutation	p.Ala680Thr(p.A680T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100980960:100980960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606G>A
AA Mutation	p.Ala536Thr(p.A536T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100977683:100977683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>T
AA Mutation	p.Leu130Phe(p.L130F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100983773:100983773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2159C>A
AA Mutation	p.Ala720Glu(p.A720E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100977653:100977653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145690277
CDS Mutation	c.358C>T
AA Mutation	p.Arg120Trp(p.R120W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100979945:100979945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199762950
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Cys(p.R361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100980960:100980960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606G>T
AA Mutation	p.Ala536Ser(p.A536S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370250
Start	100978875:100978875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528948930
CDS Mutation	c.670G>A
AA Mutation	p.Val224Met(p.V224M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370250
Start	100981207:100981207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1668C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370250
Start	100980151:100980151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370250
Start	100983309:100983309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1695A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA4G

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000370250
Start	100981202:100981202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663C>T
AA Mutation	p.Arg555Ter(p.R555*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript