Colon Cancer: Gene >> NKX2-5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329198
Start	173233077:173233077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>A
AA Mutation	p.Arg156His(p.R156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329198
Start	173233084:173233084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>C
AA Mutation	p.Glu154Gln(p.E154Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329198
Start	173232960:173232960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>A
AA Mutation	p.Arg195Gln(p.R195Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329198
Start	173233059:173233059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485A>G
AA Mutation	p.Tyr162Cys(p.Y162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329198
Start	173234860:173234860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329198
Start	173233063:173233063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Trp(p.R161W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329198
Start	173232668:173232668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NKX2-5

No Mutation Annotation!