Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ATOH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829030:93829030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772119264
CDS Mutation	c.104C>A
AA Mutation	p.Pro35Gln(p.P35Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829857:93829857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931T>G
AA Mutation	p.Leu311Val(p.L311V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829237:93829237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311A>G
AA Mutation	p.Glu104Gly(p.E104G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829008:93829008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82C>G
AA Mutation	p.Leu28Val(p.L28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829308:93829308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>G
AA Mutation	p.Leu128Val(p.L128V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829453:93829453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527A>G
AA Mutation	p.Asn176Ser(p.N176S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306011
Start	93829325:93829325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306011
Start	93829400:93829400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306011
Start	93829231:93829231(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.310delG
AA Mutation	p.Glu104SerfsTer3(p.E104Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306011
Start	93829501:93829501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.575delA
AA Mutation	p.Asp192AlafsTer111(p.D192Afs*111)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306011
Start	93829951:93829951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1030delC
AA Mutation	p.His344IlefsTer18(p.H344Ifs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ATOH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306011
Start	93829030:93829030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772119264
CDS Mutation	c.104C>A
AA Mutation	p.Pro35Gln(p.P35Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306011
Start	93829178:93829178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript