Colon Cancer: Gene >> STK10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172054573:172054573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2648T>A
AA Mutation	p.Leu883Gln(p.L883Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172106741:172106741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667C>A
AA Mutation	p.Leu223Met(p.L223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172093774:172093774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192C>A
AA Mutation	p.Pro398Thr(p.P398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172054601:172054601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2620G>A
AA Mutation	p.Glu874Lys(p.E874K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172105724:172105724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35826078
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172187997:172187997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46G>A
AA Mutation	p.Glu16Lys(p.E16K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172093720:172093720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375820809
CDS Mutation	c.1246G>A
AA Mutation	p.Val416Met(p.V416M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172096517:172096517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914A>C
AA Mutation	p.Glu305Ala(p.E305A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172082387:172082387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143251398
CDS Mutation	c.1928G>A
AA Mutation	p.Arg643His(p.R643H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172055604:172055604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2510G>A
AA Mutation	p.Arg837His(p.R837H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172082394:172082394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1921C>T
AA Mutation	p.Arg641Trp(p.R641W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172057437:172057437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2249A>G
AA Mutation	p.Gln750Arg(p.Q750R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172090330:172090330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172064738:172064738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189563470
CDS Mutation	c.2064G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172107839:172107839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172057376:172057376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2310G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172096534:172096534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000176763
Start	172090341:172090341(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1576delA
AA Mutation	p.Thr526ProfsTer15(p.T526Pfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000176763
Start	172090242:172090242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675A>T
AA Mutation	p.Arg559Ter(p.R559*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000176763
Start	172057352:172057354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2332_2334delGAG
AA Mutation	p.Glu778del(p.E778del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STK10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000176763
Start	172093577:172093577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389G>T
AA Mutation	p.Glu463Asp(p.E463D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172061263:172061263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2088G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172106631:172106631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000176763
Start	172090357:172090357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148086376
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript