Colon Cancer: Gene >> ZNF160

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53070035:53070035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759598705
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Cys(p.R167C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53068616:53068616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568622088
CDS Mutation	c.1918C>T
AA Mutation	p.Arg640Trp(p.R640W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53074260:53074260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151C>T
AA Mutation	p.His51Tyr(p.H51Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53068752:53068752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782G>T
AA Mutation	p.Lys594Asn(p.K594N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53068210:53068210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745980290
CDS Mutation	c.2324G>A
AA Mutation	p.Ser775Asn(p.S775N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53069540:53069540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757419776
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Trp(p.R332W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53074172:53074172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239G>T
AA Mutation	p.Arg80Ile(p.R80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53069645:53069645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Cys(p.R297C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53069724:53069724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53069235:53069235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53068770:53068770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1764T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53070105:53070105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53074198:53074198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418871
Start	53068531:53068531(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2003delA
AA Mutation	p.Lys668ArgfsTer53(p.K668Rfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418871
Start	53068174:53068174(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2360delA
AA Mutation	p.Lys787SerfsTer59(p.K787Sfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000418871
Start	53069452:53069452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082T>G
AA Mutation	p.Leu361Ter(p.L361*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000418871
Start	53070214:53070215(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.319_320insAATAGCT
AA Mutation	p.Ser107LysfsTer2(p.S107Kfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418871
Start	53068340:53068341(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs745909467
CDS Mutation	c.2193dupA
AA Mutation	p.Pro732ThrfsTer5(p.P732Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418871
Start	53069827:53069828(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.706_707insTG
AA Mutation	p.His236LeufsTer66(p.H236Lfs*66)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF160

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53069645:53069645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Cys(p.R297C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53068210:53068210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2324G>T
AA Mutation	p.Ser775Ile(p.S775I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53069002:53069002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532G>T
AA Mutation	p.Cys511Phe(p.C511F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53069434:53069434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100A>G
AA Mutation	p.Lys367Arg(p.K367R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000418871
Start	53068276:53068276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772717823
CDS Mutation	c.2258G>T
AA Mutation	p.Arg753Ile(p.R753I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53068851:53068851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418871
Start	53068812:53068812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267605649
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000418871
Start	53069537:53069537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756528237
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Ter(p.R333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript