Colon Cancer: Gene >> SEMA3E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83469258:83469258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>T
AA Mutation	p.Met107Ile(p.M107I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83406017:83406017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856A>G
AA Mutation	p.Thr286Ala(p.T286A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83396705:83396705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391T>A
AA Mutation	p.Ile464Asn(p.I464N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367812:83367812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2102G>A
AA Mutation	p.Ser701Asn(p.S701N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83387001:83387001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717T>C
AA Mutation	p.Phe573Leu(p.F573L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83392659:83392659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138211552
CDS Mutation	c.1563G>A
AA Mutation	p.Met521Ile(p.M521I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83368001:83368001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1913G>A
AA Mutation	p.Gly638Asp(p.G638D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83385343:83385343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778141353
CDS Mutation	c.1826C>T
AA Mutation	p.Ala609Val(p.A609V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83490224:83490224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>A
AA Mutation	p.Leu56Ile(p.L56I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83400144:83400144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>A
AA Mutation	p.Pro417His(p.P417H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83396661:83396661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>A
AA Mutation	p.Leu479Ile(p.L479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367969:83367969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1945G>A
AA Mutation	p.Ala649Thr(p.A649T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83400192:83400192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>T
AA Mutation	p.Ala401Val(p.A401V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83367901:83367901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2013G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83392662:83392662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1560C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83407130:83407130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533306215
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83400170:83400170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307792
Start	83405507:83405507(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.941delT
AA Mutation	p.Leu314CysfsTer11(p.L314Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000307792
Start	83396673:83396673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423G>T
AA Mutation	p.Glu475Ter(p.E475*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000307792
Start	83396640:83396640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456A>T
AA Mutation	p.Lys486Ter(p.K486*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA3E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83407192:83407192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777910966
CDS Mutation	c.718G>T
AA Mutation	p.Asp240Tyr(p.D240Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367621:83367621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2293C>A
AA Mutation	p.His765Asn(p.H765N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367918:83367918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1996C>T
AA Mutation	p.Arg666Cys(p.R666C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83407129:83407129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773917768
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83648532:83648532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751165516
CDS Mutation	c.11C>T
AA Mutation	p.Ala4Val(p.A4V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83387027:83387027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777600869
CDS Mutation	c.1691G>A
AA Mutation	p.Arg564Gln(p.R564Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83466580:83466580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748315427
CDS Mutation	c.358C>T
AA Mutation	p.Arg120Trp(p.R120W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83367964:83367964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1950G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000307792
Start	83396670:83396670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426G>T
AA Mutation	p.Glu476Ter(p.E476*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000307792
Start	83405972:83405972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901G>T
AA Mutation	p.Gly301Ter(p.G301*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript