Colon Cancer: Gene >> PIGK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77161371:77161371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751082508
CDS Mutation	c.737T>C
AA Mutation	p.Met246Thr(p.M246T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77169306:77169306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329T>G
AA Mutation	p.Leu110Arg(p.L110R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77206718:77206718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146489857
CDS Mutation	c.161G>A
AA Mutation	p.Arg54Gln(p.R54Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77163880:77163880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201690868
CDS Mutation	c.550G>A
AA Mutation	p.Ala184Thr(p.A184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77161655:77161655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140360373
CDS Mutation	c.641G>A
AA Mutation	p.Arg214Gln(p.R214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77166819:77166819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755599930
CDS Mutation	c.387G>T
AA Mutation	p.Glu129Asp(p.E129D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77161663:77161663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633G>A
AA Mutation	p.Met211Ile(p.M211I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370812
Start	77092407:77092407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1155T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370812
Start	77219325:77219325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370812
Start	77154562:77154562(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.873delT
AA Mutation	p.Gln292ArgfsTer8(p.Q292Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIGK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370812
Start	77161655:77161655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140360373
CDS Mutation	c.641G>A
AA Mutation	p.Arg214Gln(p.R214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370812
Start	77169278:77169278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000370812
Start	77169310:77169310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>T
AA Mutation	p.Glu109Ter(p.E109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript