Colon Cancer: Gene >> TNIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151032346:151032346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757428683
CDS Mutation	c.1817G>A
AA Mutation	p.Arg606Gln(p.R606Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151030734:151030734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1890T>A
AA Mutation	p.Asn630Lys(p.N630K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151039105:151039105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255C>G
AA Mutation	p.Leu419Val(p.L419V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151039162:151039162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198G>A
AA Mutation	p.Asp400Asn(p.D400N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151052198:151052198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689T>C
AA Mutation	p.Leu230Pro(p.L230P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151056906:151056906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777981863
CDS Mutation	c.487C>T
AA Mutation	p.Arg163Cys(p.R163C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151033621:151033621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745403030
CDS Mutation	c.1766G>A
AA Mutation	p.Arg589His(p.R589H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151035665:151035665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438C>T
AA Mutation	p.Arg480Cys(p.R480C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151032367:151032367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768467028
CDS Mutation	c.1796G>A
AA Mutation	p.Arg599His(p.R599H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315050
Start	151033779:151033779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315050
Start	151065066:151065066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760006303
CDS Mutation	c.30C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315050
Start	151030735:151030735(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1889delA
AA Mutation	p.Asn630MetfsTer24(p.N630Mfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315050
Start	151033666:151033666(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1721delC
AA Mutation	p.Pro574LeufsTer41(p.P574Lfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNIP1

No Mutation Annotation!