Colon Cancer: Gene >> SEMA3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84011065:84011065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Asp318Tyr(p.D318Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134823:84134823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376684446
CDS Mutation	c.241G>A
AA Mutation	p.Asp81Asn(p.D81N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84110532:84110532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143007146
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84002006:84002006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401G>T
AA Mutation	p.Glu467Asp(p.E467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961544:83961544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2143C>A
AA Mutation	p.Leu715Ile(p.L715I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83977177:83977177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672A>T
AA Mutation	p.Ile558Leu(p.I558L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84011240:84011240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761827491
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Cys(p.R290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84194580:84194580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7T>C
AA Mutation	p.Trp3Arg(p.W3R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83977140:83977140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1709T>C
AA Mutation	p.Leu570Ser(p.L570S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961490:83961490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138002949
CDS Mutation	c.2197C>T
AA Mutation	p.Arg733Cys(p.R733C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83963317:83963317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748G>T
AA Mutation	p.Arg583Ile(p.R583I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84011276:84011276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832A>G
AA Mutation	p.Ser278Gly(p.S278G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84002008:84002008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1399G>A
AA Mutation	p.Glu467Lys(p.E467K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134801:84134801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263T>G
AA Mutation	p.Phe88Cys(p.F88C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84194538:84194538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49A>G
AA Mutation	p.Thr17Ala(p.T17A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	83981455:83981455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780861957
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	83963268:83963268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367617715
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	83963244:83963244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1821T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	84060517:84060517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265362
Start	83961598:83961604(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2083_2089delATGACAC
AA Mutation	p.Met695LeufsTer81(p.M695Lfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961566:83961566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2121G>A
AA Mutation	p.Met707Ile(p.M707I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83963227:83963227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746887710
CDS Mutation	c.1838G>A
AA Mutation	p.Arg613Gln(p.R613Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134867:84134867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762612767
CDS Mutation	c.197G>A
AA Mutation	p.Arg66Gln(p.R66Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84110475:84110475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448C>A
AA Mutation	p.Pro150Thr(p.P150T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134823:84134823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376684446
CDS Mutation	c.241G>A
AA Mutation	p.Asp81Asn(p.D81N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961681:83961681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006A>G
AA Mutation	p.Asp669Gly(p.D669G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134844:84134844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220A>C
AA Mutation	p.Lys74Gln(p.K74Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript