Colon Cancer: Gene >> PLEKHG6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6327401:6327401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1818C>A
AA Mutation	p.Ser606Arg(p.S606R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6318869:6318869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773846283
CDS Mutation	c.1400G>A
AA Mutation	p.Arg467Gln(p.R467Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6315557:6315557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>G
AA Mutation	p.Met155Val(p.M155V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6315087:6315087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781352548
CDS Mutation	c.377G>A
AA Mutation	p.Arg126Gln(p.R126Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000011684
Start	6316403:6316403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371112449
CDS Mutation	c.755C>T
AA Mutation	p.Thr252Met(p.T252M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6326447:6326447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544A>C
AA Mutation	p.Lys515Thr(p.K515T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6315573:6315573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479G>A
AA Mutation	p.Cys160Tyr(p.C160Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6327325:6327325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1742T>C
AA Mutation	p.Val581Ala(p.V581A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000011684
Start	6317622:6317622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943A>G
AA Mutation	p.Lys315Glu(p.K315E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011684
Start	6312340:6312340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011684
Start	6312313:6312313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011684
Start	6326442:6326442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1539G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011684
Start	6317369:6317369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000011684
Start	6327376:6327377(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1793_1794insA
AA Mutation	p.Thr599HisfsTer71(p.T599Hfs*71)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000011684
Start	6327443:6327445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1862_1864delTCT
AA Mutation	p.Phe621del(p.F621del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHG6

No Mutation Annotation!