Colon Cancer: Gene >> CHSY1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178242:101178242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555C>T
AA Mutation	p.Leu519Phe(p.L519F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178164:101178164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776069033
CDS Mutation	c.1633G>A
AA Mutation	p.Asp545Asn(p.D545N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101177834:101177834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1963T>A
AA Mutation	p.Tyr655Asn(p.Y655N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178931:101178931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866T>A
AA Mutation	p.Ile289Asn(p.I289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178821:101178821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773884567
CDS Mutation	c.976G>A
AA Mutation	p.Glu326Lys(p.E326K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178545:101178545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252G>A
AA Mutation	p.Ala418Thr(p.A418T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178268:101178268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1529C>T
AA Mutation	p.Ser510Phe(p.S510F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178386:101178386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373782542
CDS Mutation	c.1411G>A
AA Mutation	p.Ala471Thr(p.A471T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101178228:101178228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1569G>T
AA Mutation	p.Lys523Asn(p.K523N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101177655:101177655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2142A>C
AA Mutation	p.Gln714His(p.Q714H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101235225:101235225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748806147
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101177846:101177846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1951G>A
AA Mutation	p.Gly651Ser(p.G651S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000254190
Start	101177441:101177441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2356G>A
AA Mutation	p.Asp786Asn(p.D786N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254190
Start	101177645:101177645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254190
Start	101178006:101178006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780922334
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254190
Start	101178387:101178387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750435215
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254190
Start	101235379:101235379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143062356
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254190
Start	101235232:101235232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764708620
CDS Mutation	c.666delG
AA Mutation	p.Pro223LeufsTer3(p.P223Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254190
Start	101177845:101177846(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1951_1952insT
AA Mutation	p.Gly651ValfsTer14(p.G651Vfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHSY1

No Mutation Annotation!