Colon Cancer: Gene >> ATP7B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51934847:51934847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4307A>G
AA Mutation	p.Asp1436Gly(p.D1436G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51974862:51974862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Gly120Cys(p.G120C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51934965:51934965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4189G>A
AA Mutation	p.Ala1397Thr(p.A1397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51944246:51944246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761147984
CDS Mutation	c.3106G>A
AA Mutation	p.Val1036Ile(p.V1036I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51960290:51960290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1979T>G
AA Mutation	p.Phe660Cys(p.F660C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51939134:51939134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3616G>A
AA Mutation	p.Val1206Met(p.V1206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51968546:51968546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1605G>T
AA Mutation	p.Glu535Asp(p.E535D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51941186:51941186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3451C>A
AA Mutation	p.Arg1151Ser(p.R1151S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51941170:51941170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773917820
CDS Mutation	c.3467G>A
AA Mutation	p.Arg1156His(p.R1156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51961903:51961903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1880T>G
AA Mutation	p.Phe627Cys(p.F627C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51974192:51974192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1028C>A
AA Mutation	p.Ser343Tyr(p.S343Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51974867:51974867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353A>G
AA Mutation	p.Asp118Gly(p.D118G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51942442:51942442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3356C>A
AA Mutation	p.Pro1119His(p.P1119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000242839
Start	51968607:51968607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>A
AA Mutation	p.Gly515Asp(p.G515D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51964910:51964910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831G>A
AA Mutation	p.Glu611Lys(p.E611K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242839
Start	51960166:51960166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242839
Start	51950393:51950393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2454G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242839
Start	51935610:51935610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4107A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ATP7B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51941105:51941105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3532A>G
AA Mutation	p.Thr1178Ala(p.T1178A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51942412:51942412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3386A>T
AA Mutation	p.Glu1129Val(p.E1129V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51939188:51939188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3562C>T
AA Mutation	p.Leu1188Phe(p.L1188F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242839
Start	51960265:51960265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2004G>T
AA Mutation	p.Met668Ile(p.M668I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242839
Start	51974275:51974275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776855440
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242839
Start	51975091:51975091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>G
Mutation Classification	Silent
Feature Type	Transcript