Colon Cancer: Gene >> NRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520407
Start	31639990:31639990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6A>T
AA Mutation	p.Arg2Ser(p.R2S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32756447:32756447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145033301
CDS Mutation	c.848G>A
AA Mutation	p.Arg283Gln(p.R283Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32756456:32756456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367543164
CDS Mutation	c.857G>A
AA Mutation	p.Arg286Gln(p.R286Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763759:32763759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199688344
CDS Mutation	c.1280C>T
AA Mutation	p.Ala427Val(p.A427V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764232:32764232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1753G>T
AA Mutation	p.Asp585Tyr(p.D585Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32760251:32760251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113C>G
AA Mutation	p.Ile371Met(p.I371M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763879:32763879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774365052
CDS Mutation	c.1400C>T
AA Mutation	p.Ala467Val(p.A467V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000523534
Start	31640573:31640573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148G>A
AA Mutation	p.Gly50Arg(p.G50R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764115:32764115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114185597
CDS Mutation	c.1636C>T
AA Mutation	p.Arg546Trp(p.R546W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32728035:32728035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589T>C
AA Mutation	p.Phe197Leu(p.F197L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32605572:32605572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>A
AA Mutation	p.Leu97Ile(p.L97I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32756434:32756434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367543163
CDS Mutation	c.835C>T
AA Mutation	p.Arg279Trp(p.R279W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32595864:32595864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137A>T
AA Mutation	p.Glu46Val(p.E46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32759372:32759372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997T>C
AA Mutation	p.Ser333Pro(p.S333P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32728071:32728071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625T>A
AA Mutation	p.Leu209Met(p.L209M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32760343:32760343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205A>C
AA Mutation	p.Asn402Thr(p.N402T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32760247:32760247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109T>C
AA Mutation	p.Val370Ala(p.V370A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32728047:32728047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>C
AA Mutation	p.Asp201His(p.D201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32763829:32763829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752389906
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523534
Start	31640572:31640572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32763844:32763844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1365C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520407
Start	31640005:31640005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32742035:32742035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523534
Start	31640458:31640458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764117626
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000405005
Start	32595993:32595993(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.272delA
AA Mutation	p.Lys91SerfsTer24(p.K91Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000405005
Start	32756455:32756455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856C>T
AA Mutation	p.Arg286Ter(p.R286*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000405005
Start	32760267:32760267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>T
AA Mutation	p.Glu377Ter(p.E377*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763958:32763958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1479T>G
AA Mutation	p.His493Gln(p.H493Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764057:32764057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1578A>C
AA Mutation	p.Glu526Asp(p.E526D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763767:32763767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288A>T
AA Mutation	p.Thr430Ser(p.T430S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32595909:32595909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182C>A
AA Mutation	p.Ser61Tyr(p.S61Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32756511:32756511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.912G>T
AA Mutation	p.Glu304Asp(p.E304D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32728064:32728064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768024564
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript