Colon Cancer: Gene >> FKBP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321562
Start	41818515:41818515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782261801
CDS Mutation	c.715G>A
AA Mutation	p.Glu239Lys(p.E239K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321562
Start	41817102:41817102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371079363
CDS Mutation	c.290G>A
AA Mutation	p.Arg97His(p.R97H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321562
Start	41817101:41817101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Cys(p.R97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321562
Start	41819600:41819600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.988C>A
AA Mutation	p.Leu330Met(p.L330M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321562
Start	41819654:41819654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042G>A
AA Mutation	p.Ala348Thr(p.A348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321562
Start	41819226:41819226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321562
Start	41819641:41819641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1034delC
AA Mutation	p.Pro345ArgfsTer20(p.P345Rfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321562
Start	41819307:41819307(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.831delC
AA Mutation	p.Gly278AlafsTer20(p.G278Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321562
Start	41822285:41822285(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1628delC
AA Mutation	p.Pro543LeufsTer5(p.P543Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000321562
Start	41822400:41822400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1741G>T
AA Mutation	p.Glu581Ter(p.E581*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FKBP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321562
Start	41821810:41821810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140883152
CDS Mutation	c.1556C>T
AA Mutation	p.Pro519Leu(p.P519L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321562
Start	41821076:41821076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571808781
CDS Mutation	c.1386C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321562
Start	41821744:41821745(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1490_1491insT
AA Mutation	p.Trp497CysfsTer11(p.W497Cfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript