Colon Cancer: Gene >> NUDT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77741879:77741879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755091970
CDS Mutation	c.646C>A
AA Mutation	p.Leu216Ile(p.L216I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77735870:77735870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765625065
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000268533
Start	77725431:77725431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36A>C
AA Mutation	p.Arg12Ser(p.R12S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77735978:77735978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340C>T
AA Mutation	p.Leu114Phe(p.L114F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77741808:77741808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76004401
CDS Mutation	c.575C>T
AA Mutation	p.Thr192Met(p.T192M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77735873:77735873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235G>A
AA Mutation	p.Asp79Asn(p.D79N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77725517:77725517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122C>A
AA Mutation	p.Ser41Tyr(p.S41Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268533
Start	77725455:77725455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268533
Start	77741641:77741641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375405359
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268533
Start	77741847:77741847(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762359424
CDS Mutation	c.621delA
AA Mutation	p.Lys207AsnfsTer14(p.K207Nfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268533
Start	77741846:77741847(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs528673952
CDS Mutation	c.621dupA
AA Mutation	p.Pro208ThrfsTer4(p.P208Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268533
Start	77725456:77725457(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.64dupC
AA Mutation	p.Arg22ProfsTer6(p.R22Pfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NUDT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268533
Start	77725448:77725448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53A>G
AA Mutation	p.Asp18Gly(p.D18G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268533
Start	77741755:77741755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>A
Mutation Classification	Silent
Feature Type	Transcript