Colon Cancer: Gene >> SEMA3G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52441603:52441603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>A
AA Mutation	p.Arg213His(p.R213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52442578:52442578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746088829
CDS Mutation	c.320G>A
AA Mutation	p.Arg107Gln(p.R107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52440773:52440773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201087157
CDS Mutation	c.979G>A
AA Mutation	p.Ala327Thr(p.A327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52441275:52441275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000231721
Start	52442907:52442907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116A>G
AA Mutation	p.Asp39Gly(p.D39G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52442778:52442778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767520734
CDS Mutation	c.245G>A
AA Mutation	p.Arg82Gln(p.R82Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52435700:52435700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2252G>T
AA Mutation	p.Arg751Met(p.R751M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52438939:52438939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490T>C
AA Mutation	p.Met497Thr(p.M497T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231721
Start	52441390:52441390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368237957
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231721
Start	52440458:52440458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199844708
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231721
Start	52435627:52435627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776988299
CDS Mutation	c.2325G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231721
Start	52440977:52440977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771113427
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231721
Start	52440759:52440759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000231721
Start	52435818:52435818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2134C>T
AA Mutation	p.Gln712Ter(p.Q712*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000231721
Start	52442579:52442579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Ter(p.R107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_lost
Transcription ID	ENST00000231721
Start	52435603:52435603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2349G>T
AA Mutation	p.Ter783TyrextTer51(p.*783Yext*51)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA3G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52435628:52435628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759858543
CDS Mutation	c.2324C>T
AA Mutation	p.Thr775Met(p.T775M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231721
Start	52438943:52438943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538568921
CDS Mutation	c.1486G>A
AA Mutation	p.Glu496Lys(p.E496K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000231721
Start	52441649:52441649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759458121
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Ter(p.R198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript