Colon Cancer: Gene >> NRXN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78651243:78651243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19T>G
AA Mutation	p.Phe7Val(p.F7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78968331:78968331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756589243
CDS Mutation	c.2008G>A
AA Mutation	p.Glu670Lys(p.E670K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79861579:79861579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746905701
CDS Mutation	c.1529C>T
AA Mutation	p.Pro510Leu(p.P510L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79280521:79280521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772513292
CDS Mutation	c.230C>T
AA Mutation	p.Ser77Phe(p.S77F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79805165:79805165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963C>A
AA Mutation	p.Asp321Glu(p.D321E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79663875:79663875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527T>C
AA Mutation	p.Val176Ala(p.V176A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78803749:78803749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055C>T
AA Mutation	p.Thr352Met(p.T352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79467274:79467274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301C>T
AA Mutation	p.Pro101Ser(p.P101S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79280310:79280310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141234557
CDS Mutation	c.19G>A
AA Mutation	p.Ala7Thr(p.A7T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79697693:79697693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78714783:78714783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201888810
CDS Mutation	c.569C>T
AA Mutation	p.Thr190Met(p.T190M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79861702:79861702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1652C>G
AA Mutation	p.Ala551Gly(p.A551G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78803767:78803767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1073C>T
AA Mutation	p.Ala358Val(p.A358V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78968335:78968335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137943866
CDS Mutation	c.2012G>A
AA Mutation	p.Arg671His(p.R671H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78968283:78968283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140301017
CDS Mutation	c.1960C>T
AA Mutation	p.Arg654Cys(p.R654C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000557594
Start	79467283:79467283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Asp104Asn(p.D104N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78709433:78709433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Pro107Ser(p.P107S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78988082:78988082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2084G>T
AA Mutation	p.Trp695Leu(p.W695L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78957340:78957340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>A
AA Mutation	p.Val419Met(p.V419M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78709523:78709523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200274508
CDS Mutation	c.409G>A
AA Mutation	p.Val137Met(p.V137M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78966315:78966315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567T>C
AA Mutation	p.Phe523Leu(p.F523L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78714780:78714780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369032353
CDS Mutation	c.566G>A
AA Mutation	p.Arg189His(p.R189H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78714950:78714950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764624479
CDS Mutation	c.736C>T
AA Mutation	p.Arg246Cys(p.R246C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78709265:78709265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748055286
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Trp(p.R51W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554719
Start	78968285:78968285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1962C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554719
Start	78715105:78715105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756301310
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554719
Start	78709567:78709567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557594
Start	79663858:79663858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144173846
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554719
Start	78966095:78966095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557594
Start	79861793:79861793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779505235
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554719
Start	78966104:78966104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765527436
CDS Mutation	c.1356C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000554719
Start	78803793:78803793(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1104delG
AA Mutation	p.Arg369ValfsTer8(p.R369Vfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NRXN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78968284:78968284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368490229
CDS Mutation	c.1961G>A
AA Mutation	p.Arg654His(p.R654H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78709516:78709516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402C>A
AA Mutation	p.Phe134Leu(p.F134L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78968178:78968178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1855C>T
AA Mutation	p.Leu619Phe(p.L619F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000554719
Start	78988121:78988121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2123C>A
AA Mutation	p.Ser708Tyr(p.S708Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557594
Start	79861919:79861919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1869C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557594
Start	79280351:79280351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript