Colon Cancer: Gene >> METAP1D

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000315796
Start	172080330:172080330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138526406
CDS Mutation	c.932C>T
AA Mutation	p.Ser311Leu(p.S311L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315796
Start	172063831:172063831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751521756
CDS Mutation	c.319G>A
AA Mutation	p.Val107Ile(p.V107I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315796
Start	172080341:172080341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943G>A
AA Mutation	p.Glu315Lys(p.E315K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315796
Start	172065725:172065725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470A>G
AA Mutation	p.Asn157Ser(p.N157S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315796
Start	172061577:172061577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>A
AA Mutation	p.Phe40Leu(p.F40L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315796
Start	172063736:172063736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745357105
CDS Mutation	c.224C>T
AA Mutation	p.Thr75Met(p.T75M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315796
Start	172070999:172070999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315796
Start	172080373:172080373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315796
Start	172080370:172080370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> METAP1D

No Mutation Annotation!