Colon Cancer: Gene >> AVL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318709
Start	32575982:32575982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1598G>T
AA Mutation	p.Gly533Val(p.G533V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318709
Start	32580818:32580818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1759G>A
AA Mutation	p.Glu587Lys(p.E587K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318709
Start	32573335:32573335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141983074
CDS Mutation	c.1487C>T
AA Mutation	p.Thr496Met(p.T496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318709
Start	32570058:32570058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571836783
CDS Mutation	c.1254T>G
AA Mutation	p.His418Gln(p.H418Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318709
Start	32543141:32543141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>A
AA Mutation	p.Val32Ile(p.V32I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318709
Start	32573409:32573409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1561C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AVL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318709
Start	32552292:32552292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526C>A
AA Mutation	p.Leu176Ile(p.L176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318709
Start	32576065:32576065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1681A>C
AA Mutation	p.Asn561His(p.N561H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript