Colon Cancer: Gene >> SEMA4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90217785:90217785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>A
AA Mutation	p.Ala114Thr(p.A114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90225130:90225130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746145639
CDS Mutation	c.1357C>T
AA Mutation	p.Arg453Cys(p.R453C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90227633:90227633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1765G>T
AA Mutation	p.Val589Leu(p.V589L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90227988:90227988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746051036
CDS Mutation	c.1859G>A
AA Mutation	p.Arg620Gln(p.R620Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90225029:90225029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1256T>C
AA Mutation	p.Val419Ala(p.V419A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411539
Start	90225132:90225132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199919293
CDS Mutation	c.1359C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411539
Start	90221026:90221026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411539
Start	90228013:90228013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776296311
CDS Mutation	c.1884C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411539
Start	90228004:90228004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772043069
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000411539
Start	90228507:90228508(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759756102
CDS Mutation	c.2384dupC
AA Mutation	p.Ser797ValfsTer6(p.S797Vfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000411539
Start	90228384:90228386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2255_2257delAAT
AA Mutation	p.Glu752_Cys753delinsGly(p.E752_C753delinsG)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90228618:90228618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759611815
CDS Mutation	c.2489C>T
AA Mutation	p.Ser830Leu(p.S830L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000411539
Start	90217594:90217594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313T>A
AA Mutation	p.Tyr105Asn(p.Y105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411539
Start	90221002:90221002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758335362
CDS Mutation	c.504G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000411539
Start	90228384:90228386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2255_2257delAAT
AA Mutation	p.Glu752_Cys753delinsGly(p.E752_C753delinsG)
Mutation Classification	In_Frame_Del
Feature Type	Transcript