Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SEMA6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116447275:116447275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2431C>A
AA Mutation	p.His811Asn(p.H811N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116478699:116478699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270G>C
AA Mutation	p.Ala424Pro(p.A424P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116446911:116446911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2795C>T
AA Mutation	p.Thr932Ile(p.T932I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116495505:116495505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>T
AA Mutation	p.His118Tyr(p.H118Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116478678:116478678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1291C>T
AA Mutation	p.Pro431Ser(p.P431S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116447764:116447764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778751794
CDS Mutation	c.1942G>A
AA Mutation	p.Val648Ile(p.V648I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116447391:116447391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764283270
CDS Mutation	c.2315G>A
AA Mutation	p.Arg772His(p.R772H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116446672:116446672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3034C>T
AA Mutation	p.Pro1012Ser(p.P1012S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116446713:116446713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781118630
CDS Mutation	c.2993C>T
AA Mutation	p.Ser998Leu(p.S998L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116447451:116447451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2255T>C
AA Mutation	p.Leu752Pro(p.L752P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116467601:116467601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876A>C
AA Mutation	p.Asn626His(p.N626H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116488960:116488960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773059701
CDS Mutation	c.583G>A
AA Mutation	p.Ala195Thr(p.A195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116446701:116446701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200942463
CDS Mutation	c.3005G>A
AA Mutation	p.Arg1002His(p.R1002H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116447246:116447246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2460C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116446697:116446697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559240638
CDS Mutation	c.3009G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116480190:116480190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369918649
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116491777:116491777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116488907:116488907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373510249
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116480202:116480202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116446619:116446619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116447243:116447243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2463G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116446739:116446739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2967C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343348
Start	116482548:116482548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343348
Start	116447069:116447069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2637delC
AA Mutation	p.Val881PhefsTer20(p.V881Ffs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343348
Start	116446670:116446670(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs751600344
CDS Mutation	c.3036delC
AA Mutation	p.Lys1013AsnfsTer11(p.K1013Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343348
Start	116446669:116446670(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3036dupC
AA Mutation	p.Lys1013GlnfsTer15(p.K1013Qfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343348
Start	116446955:116446956(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2750dupA
AA Mutation	p.Arg918GlufsTer23(p.R918Efs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343348
Start	116446737:116446738(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2968_2969insTGTAC
AA Mutation	p.Asn990MetfsTer8(p.N990Mfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116447718:116447718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988C>G
AA Mutation	p.Ala663Gly(p.A663G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343348
Start	116446935:116446935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2771C>T
AA Mutation	p.Ser924Leu(p.S924L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343348
Start	116447068:116447069(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749631581
CDS Mutation	c.2637dupC
AA Mutation	p.Lys880GlnfsTer36(p.K880Qfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript