Colon Cancer: Gene >> PQLC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375153
Start	19317736:19317736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59A>G
AA Mutation	p.Gln20Arg(p.Q20R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375153
Start	19317783:19317783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546350739
CDS Mutation	c.106G>A
AA Mutation	p.Glu36Lys(p.E36K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375153
Start	19324674:19324674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755077935
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375153
Start	19327291:19327291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756272440
CDS Mutation	c.683C>T
AA Mutation	p.Thr228Met(p.T228M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375153
Start	19324744:19324744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375153
Start	19324648:19324648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375153
Start	19326581:19326581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375153
Start	19327307:19327307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376864579
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375153
Start	19326581:19326582(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.579_580dupGT
AA Mutation	p.Leu194CysfsTer31(p.L194Cfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000375153
Start	19327413:19327413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758915063
CDS Mutation	c.804+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PQLC2

No Mutation Annotation!