Colon Cancer: Gene >> CA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378357
Start	35674192:35674192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233C>T
AA Mutation	p.Pro78Leu(p.P78L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378357
Start	35679193:35679193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916A>G
AA Mutation	p.Thr306Ala(p.T306A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000378357
Start	35679998:35679998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210G>A
AA Mutation	p.Val404Ile(p.V404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378357
Start	35679962:35679962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378357
Start	35675796:35675796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Ala157Thr(p.A157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378357
Start	35679861:35679861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073C>T
AA Mutation	p.Thr358Ile(p.T358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378357
Start	35679992:35679992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204G>A
AA Mutation	p.Glu402Lys(p.E402K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378357
Start	35679919:35679919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763934915
CDS Mutation	c.1131G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378357
Start	35680805:35680805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754134463
CDS Mutation	c.1290G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CA9

No Mutation Annotation!