Colon Cancer: Gene >> PHKG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000563588
Start	30751221:30751221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756052327
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000563588
Start	30751126:30751126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373732367
CDS Mutation	c.116G>A
AA Mutation	p.Arg39His(p.R39H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000563588
Start	30751141:30751141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778737777
CDS Mutation	c.131G>A
AA Mutation	p.Arg44Gln(p.R44Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000563588
Start	30756907:30756907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532137455
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344Gln(p.R344Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000563588
Start	30753456:30753456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Gln(p.R152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000563588
Start	30753274:30753274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000563588
Start	30751109:30751109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000563588
Start	30756696:30756696(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.913delC
AA Mutation	p.Arg305AlafsTer19(p.R305Afs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PHKG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000563588
Start	30751263:30751263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535265672
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript