Colon Cancer: Gene >> ANO9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	428766:428766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976T>C
AA Mutation	p.Ser326Pro(p.S326P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	419639:419639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765622452
CDS Mutation	c.1877G>A
AA Mutation	p.Arg626Gln(p.R626Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	429620:429620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145473999
CDS Mutation	c.865C>T
AA Mutation	p.Arg289Cys(p.R289C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	418456:418456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2264G>A
AA Mutation	p.Gly755Asp(p.G755D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	428823:428823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919G>A
AA Mutation	p.Glu307Lys(p.E307K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	428790:428790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952T>C
AA Mutation	p.Tyr318His(p.Y318H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332826
Start	418563:418563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777464444
CDS Mutation	c.2157C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332826
Start	428484:428484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332826
Start	419629:419629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1887C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332826
Start	418789:418789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2061delC
AA Mutation	p.Asp688IlefsTer44(p.D688Ifs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000332826
Start	428140:428140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282C>T
AA Mutation	p.Gln428Ter(p.Q428*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332826
Start	433356:433357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs773213308
CDS Mutation	c.307dupC
AA Mutation	p.His103ProfsTer34(p.H103Pfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ANO9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332826
Start	433453:433453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775078390
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript