Colon Cancer: Gene >> TNNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236918
Start	201365276:201365276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326T>C
AA Mutation	p.Leu109Pro(p.L109P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000236918
Start	201364315:201364315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730881123
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Trp(p.R158W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000236918
Start	201365620:201365620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284T>A
AA Mutation	p.Val95Glu(p.V95E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000236918
Start	201365297:201365297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305G>T
AA Mutation	p.Arg102Leu(p.R102L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000236918
Start	201364342:201364342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397516465
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Cys(p.R149C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236918
Start	201367790:201367790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236918
Start	201359243:201359243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45503195
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236918
Start	201365302:201365302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236918
Start	201365619:201365620(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.284_285delTG
AA Mutation	p.Val95GlyfsTer3(p.V95Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000236918
Start	201365286:201365286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>T
AA Mutation	p.Glu106Ter(p.E106*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNNT2

No Mutation Annotation!