Colon Cancer: Gene >> STMN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265770
Start	27241211:27241211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>G
AA Mutation	p.Glu54Gly(p.E54G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265770
Start	27241235:27241235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137T>C
AA Mutation	p.Val46Ala(p.V46A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265770
Start	27242451:27242451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55T>C
AA Mutation	p.Phe19Leu(p.F19L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265770
Start	27241098:27241098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Glu92Lys(p.E92K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265770
Start	27241212:27241212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265770
Start	27241195:27241195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265770
Start	27240151:27240151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STMN4

No Mutation Annotation!