Colon Cancer: Gene >> KDM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286096
Start	27220460:27220460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534702057
CDS Mutation	c.1061C>T
AA Mutation	p.Thr354Met(p.T354M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286096
Start	27210139:27210139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>A
AA Mutation	p.His6Asn(p.H6N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286096
Start	27210397:27210397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201598678
CDS Mutation	c.274C>T
AA Mutation	p.Arg92Cys(p.R92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286096
Start	27220711:27220711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232T>G
AA Mutation	p.Val411Gly(p.V411G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286096
Start	27220683:27220683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141999943
CDS Mutation	c.1204G>A
AA Mutation	p.Val402Met(p.V402M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286096
Start	27213596:27213596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763893122
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286096
Start	27215959:27215959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286096
Start	27210318:27210318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286096
Start	27210531:27210531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000286096
Start	27218960:27218960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KDM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286096
Start	27220658:27220658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>A
AA Mutation	p.Phe393Leu(p.F393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000286096
Start	27213584:27213584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript