Colon Cancer: Gene >> NLGN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	173604981:173604981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383A>C
AA Mutation	p.Glu128Ala(p.E128A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	173604942:173604942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344C>A
AA Mutation	p.Pro115His(p.P115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174281184:174281184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2353C>T
AA Mutation	p.Pro785Ser(p.P785S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174275490:174275490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822T>G
AA Mutation	p.His274Gln(p.H274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279392:174279392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391A>G
AA Mutation	p.Gln464Arg(p.Q464R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174281011:174281011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2180A>C
AA Mutation	p.Glu727Ala(p.E727A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279517:174279517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516G>A
AA Mutation	p.Gly506Arg(p.G506R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279013:174279013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012C>T
AA Mutation	p.Pro338Ser(p.P338S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279542:174279542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541G>T
AA Mutation	p.Gly514Val(p.G514V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	173604795:173604795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197A>C
AA Mutation	p.Lys66Thr(p.K66T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279383:174279383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201897162
CDS Mutation	c.1382C>T
AA Mutation	p.Thr461Met(p.T461M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279103:174279103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>A
AA Mutation	p.Asp368Asn(p.D368N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174275514:174275514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846C>A
AA Mutation	p.Ser282Arg(p.S282R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000457714
Start	174280511:174280511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747826638
CDS Mutation	c.1680G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000457714
Start	173807732:173807732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000457714
Start	174279447:174279447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000457714
Start	174275438:174275438(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.774delT
AA Mutation	p.Phe258LeufsTer13(p.F258Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000457714
Start	173807817:173807817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Ter(p.R211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000457714
Start	174279453:174279453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452C>G
AA Mutation	p.Tyr484Ter(p.Y484*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000457714
Start	174279052:174279052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051C>T
AA Mutation	p.Arg351Ter(p.R351*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NLGN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	173604839:173604839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241C>T
AA Mutation	p.Leu81Phe(p.L81F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174281092:174281092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261T>A
AA Mutation	p.Leu754His(p.L754H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174279418:174279418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1417G>T
AA Mutation	p.Ala473Ser(p.A473S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	173605049:173605049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Glu151Lys(p.E151K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174275409:174275409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761909514
CDS Mutation	c.741C>A
AA Mutation	p.Phe247Leu(p.F247L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000457714
Start	174275378:174275378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>A
AA Mutation	p.Ala237Asp(p.A237D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript