Colon Cancer: Gene >> GUCY2C

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261170
Start	14669722:14669722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282G>A
AA Mutation	p.Gly428Ser(p.G428S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14661009:14661009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>T
AA Mutation	p.Leu446Phe(p.L446F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14616677:14616677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2926G>A
AA Mutation	p.Glu976Lys(p.E976K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14641124:14641124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201111235
CDS Mutation	c.2026C>T
AA Mutation	p.Arg676Trp(p.R676W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14688060:14688060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221T>C
AA Mutation	p.Leu74Pro(p.L74P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14696415:14696415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34T>C
AA Mutation	p.Ser12Pro(p.S12P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14669725:14669725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150939711
CDS Mutation	c.1279C>T
AA Mutation	p.Arg427Trp(p.R427W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14651436:14651436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1681A>C
AA Mutation	p.Ile561Leu(p.I561L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14661015:14661015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1330G>A
AA Mutation	p.Val444Met(p.V444M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14616682:14616682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2921G>T
AA Mutation	p.Arg974Ile(p.R974I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261170
Start	14645231:14645231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1795A>G
AA Mutation	p.Lys599Glu(p.K599E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14641142:14641142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587784572
CDS Mutation	c.2008G>A
AA Mutation	p.Ala670Thr(p.A670T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14643688:14643688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1816T>C
AA Mutation	p.Ser606Pro(p.S606P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261170
Start	14669724:14669724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142517628
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427Gln(p.R427Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261170
Start	14651446:14651446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261170
Start	14686187:14686187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261170
Start	14651980:14651980(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1584delA
AA Mutation	p.Lys528AsnfsTer4(p.K528Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261170
Start	14625895:14625895(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2270delA
AA Mutation	p.Asn757MetfsTer8(p.N757Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261170
Start	14613274:14613275(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3064_3065insCAGC
AA Mutation	p.Leu1022SerfsTer34(p.L1022Sfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GUCY2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261170
Start	14625872:14625872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2293A>C
AA Mutation	p.Ile765Leu(p.I765L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript