Colon Cancer: Gene >> STON1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582030:48582030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771873180
CDS Mutation	c.1397G>A
AA Mutation	p.Arg466Gln(p.R466Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582428:48582428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147440328
CDS Mutation	c.1795C>T
AA Mutation	p.Arg599Cys(p.R599C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582327:48582327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694G>A
AA Mutation	p.Cys565Tyr(p.C565Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582346:48582346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1713C>A
AA Mutation	p.His571Gln(p.H571Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48580929:48580929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.296C>T
AA Mutation	p.Thr99Ile(p.T99I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48581598:48581598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965T>C
AA Mutation	p.Ile322Thr(p.I322T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582441:48582441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808T>C
AA Mutation	p.Leu603Pro(p.L603P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582322:48582322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1689G>T
AA Mutation	p.Arg563Ser(p.R563S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48591680:48591680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958A>G
AA Mutation	p.Tyr653Cys(p.Y653C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48582180:48582180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150634127
CDS Mutation	c.1547G>A
AA Mutation	p.Arg516His(p.R516H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48595280:48595280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770568145
CDS Mutation	c.2186T>C
AA Mutation	p.Ile729Thr(p.I729T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48581168:48581168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535G>A
AA Mutation	p.Asp179Asn(p.D179N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48591836:48591836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2114G>A
AA Mutation	p.Arg705Gln(p.R705Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48582025:48582025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200191646
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48581005:48581005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48595299:48595299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2205G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48582292:48582292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1659G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404752
Start	48581176:48581176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.547delT
AA Mutation	p.Ser183GlnfsTer39(p.S183Qfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404752
Start	48582060:48582060(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1433delA
AA Mutation	p.Lys478ArgfsTer14(p.K478Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000404752
Start	48582116:48582116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483G>T
AA Mutation	p.Glu495Ter(p.E495*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000404752
Start	48581738:48581738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>T
AA Mutation	p.Glu369Ter(p.E369*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STON1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404752
Start	48581282:48581282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>A
AA Mutation	p.Asp217Asn(p.D217N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48581389:48581389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48591720:48591720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1998T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404752
Start	48582025:48582025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200191646
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000404752
Start	48582035:48582035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402G>T
AA Mutation	p.Glu468Ter(p.E468*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript