Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> H2AFY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000510038
Start	135343281:135343281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932T>G
AA Mutation	p.Phe311Cys(p.F311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000510038
Start	135370138:135370138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000510038
Start	135360572:135360572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147908999
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000510038
Start	135370054:135370054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000510038
Start	135369488:135369488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.395delC
AA Mutation	p.Pro132GlnfsTer66(p.P132Qfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000510038
Start	135369595:135369595(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.288delA
AA Mutation	p.Gly97GlufsTer4(p.G97Efs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000510038
Start	135389016:135389016(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.78delG
AA Mutation	p.Arg27GlyfsTer30(p.R27Gfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000510038
Start	135369462:135369462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421C>T
AA Mutation	p.Gln141Ter(p.Q141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> H2AFY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000510038
Start	135334997:135334997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098G>C
AA Mutation	p.Met366Ile(p.M366I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000510038
Start	135388995:135388995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>T
AA Mutation	p.Lys33Asn(p.K33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000510038
Start	135388944:135388944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript