Colon Cancer: Gene >> PRKAA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56704288:56704288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106G>T
AA Mutation	p.Arg369Met(p.R369M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56707598:56707598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544C>T
AA Mutation	p.Ser515Phe(p.S515F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56707651:56707651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597G>T
AA Mutation	p.Gly533Cys(p.G533C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56707622:56707622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568G>A
AA Mutation	p.Ser523Asn(p.S523N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56706195:56706195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397T>G
AA Mutation	p.Leu466Arg(p.L466R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56704402:56704402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220G>A
AA Mutation	p.Arg407Gln(p.R407Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56706171:56706171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373A>G
AA Mutation	p.Tyr458Cys(p.Y458C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56674422:56674422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136A>C
AA Mutation	p.Ile46Leu(p.I46L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371244
Start	56693811:56693811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367787992
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371244
Start	56704061:56704061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371244
Start	56707581:56707581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371244
Start	56693844:56693844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371244
Start	56707596:56707597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1547_1548delTC
AA Mutation	p.Leu516HisfsTer25(p.L516Hfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371244
Start	56691421:56691421(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.270delT
AA Mutation	p.Phe90LeufsTer3(p.F90Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371244
Start	56707668:56707668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1620delT
AA Mutation	p.Phe540LeufsTer7(p.F540Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRKAA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56704402:56704402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220G>A
AA Mutation	p.Arg407Gln(p.R407Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371244
Start	56706113:56706113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Cys(p.R439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371244
Start	56692456:56692456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201580595
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript