Colon Cancer: Gene >> PLEKHG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6470517:6470517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1837G>A
AA Mutation	p.Glu613Lys(p.E613K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6470257:6470257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1947G>A
AA Mutation	p.Met649Ile(p.M649I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6473439:6473439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Cys(p.R259C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6468530:6468530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2474C>T
AA Mutation	p.Thr825Met(p.T825M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000400915
Start	6473252:6473252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Arg321Gln(p.R321Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6470271:6470271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933G>T
AA Mutation	p.Gly645Trp(p.G645W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6476006:6476006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242G>A
AA Mutation	p.Arg81Gln(p.R81Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6469561:6469561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2084G>A
AA Mutation	p.Arg695Gln(p.R695Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6474072:6474072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>T
AA Mutation	p.Gly234Trp(p.G234W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6496535:6496535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6470765:6470765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1680G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6475501:6475501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6474073:6474073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567059799
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6467983:6467983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3021C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6468226:6468226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373880458
CDS Mutation	c.2778G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000400915
Start	6468455:6468455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2549C>A
AA Mutation	p.Ser850Ter(p.S850*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000400915
Start	6475055:6475057(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781153386
CDS Mutation	c.460_462delAAG
AA Mutation	p.Lys154del(p.K154del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000400915
Start	6475950:6475951(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs765603114
CDS Mutation	c.295_297dupGAG
AA Mutation	p.Glu99dup(p.E99dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6467568:6467568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3184G>A
AA Mutation	p.Val1062Ile(p.V1062I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400915
Start	6474518:6474518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540G>T
AA Mutation	p.Gln180His(p.Q180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400915
Start	6473121:6473121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750570012
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript