Colon Cancer: Gene >> CALML6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307786
Start	1916543:1916543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>A
AA Mutation	p.Leu61Ile(p.L61I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307786
Start	1916839:1916839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760650110
CDS Mutation	c.341C>T
AA Mutation	p.Ala114Val(p.A114V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307786
Start	1916989:1916989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147764999
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307786
Start	1916980:1916980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307786
Start	1916771:1916771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367726631
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307786
Start	1916527:1916527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148438395
CDS Mutation	c.165G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CALML6

No Mutation Annotation!