Colon Cancer: Gene >> TIMP3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000266085
Start	32858019:32858019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Cys(p.R107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32858113:32858113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Gln(p.R138Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32859258:32859258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773990898
CDS Mutation	c.517G>A
AA Mutation	p.Gly173Ser(p.G173S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32858121:32858121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421C>A
AA Mutation	p.Leu141Met(p.L141M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32857285:32857285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241T>C
AA Mutation	p.Tyr81His(p.Y81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32858094:32858094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Cys(p.R132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32857357:32857357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313A>C
AA Mutation	p.Thr105Pro(p.T105P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266085
Start	32849481:32849481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>A
AA Mutation	p.Leu51Met(p.L51M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266085
Start	32859263:32859263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266085
Start	32857290:32857290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266085
Start	32859344:32859344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266085
Start	32859337:32859337(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.602delC
AA Mutation	p.Pro201ArgfsTer26(p.P201Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266085
Start	32859336:32859337(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749890843
CDS Mutation	c.602dupC
AA Mutation	p.Asp202GlyfsTer2(p.D202Gfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266085
Start	32859335:32859336(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.594_595insC
AA Mutation	p.Ala199ArgfsTer5(p.A199Rfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TIMP3

No Mutation Annotation!