Colon Cancer: Gene >> APOL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409652
Start	35658949:35658949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385A>G
AA Mutation	p.Thr129Ala(p.T129A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409652
Start	35658780:35658780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>T
AA Mutation	p.Lys72Asn(p.K72N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409652
Start	35659498:35659498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780403475
CDS Mutation	c.934G>A
AA Mutation	p.Glu312Lys(p.E312K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409652
Start	35659560:35659560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547112156
CDS Mutation	c.996G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> APOL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409652
Start	35659351:35659351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775222843
CDS Mutation	c.787G>A
AA Mutation	p.Ala263Thr(p.A263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409652
Start	35659546:35659546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982C>T
Mutation Classification	Silent
Feature Type	Transcript