Colon Cancer: Gene >> GNAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50194780:50194780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878A>G
AA Mutation	p.Glu293Gly(p.E293G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50193839:50193839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536G>A
AA Mutation	p.Gly179Asp(p.G179D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50193401:50193401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50193339:50193339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224A>G
AA Mutation	p.Gln75Arg(p.Q75R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50194523:50194523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731A>G
AA Mutation	p.His244Arg(p.H244R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50191745:50191745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20C>T
AA Mutation	p.Ala7Val(p.A7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50193811:50193811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149647295
CDS Mutation	c.508G>A
AA Mutation	p.Val170Met(p.V170M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232461
Start	50193818:50193818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232461
Start	50191791:50191791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367565550
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232461
Start	50193628:50193628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544821663
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232461
Start	50194790:50194790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232461
Start	50191753:50191753(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.29delA
AA Mutation	p.Lys10SerfsTer10(p.K10Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232461
Start	50193378:50193379(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.264_268dupCATCC
AA Mutation	p.Gln90ProfsTer16(p.Q90Pfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GNAT1

No Mutation Annotation!