Colon Cancer: Gene >> ANO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70187973:70187973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2930C>A
AA Mutation	p.Pro977His(p.P977H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70171013:70171013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2324C>T
AA Mutation	p.Pro775Leu(p.P775L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70171012:70171012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2323C>T
AA Mutation	p.Pro775Ser(p.P775S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70163321:70163321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371196052
CDS Mutation	c.1931G>A
AA Mutation	p.Arg644His(p.R644H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70108375:70108375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768285449
CDS Mutation	c.770C>T
AA Mutation	p.Thr257Met(p.T257M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70187828:70187828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2785C>A
AA Mutation	p.Leu929Ile(p.L929I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70180050:70180050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2397C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70126079:70126079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70161704:70161704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1863C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70087991:70087991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557246681
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70161265:70161265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70182537:70182537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140131906
CDS Mutation	c.2439G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70126169:70126169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570844488
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70132048:70132048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374544085
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70126106:70126106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201448245
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70105764:70105764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355303
Start	70104032:70104032(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.580delA
AA Mutation	p.Ile194SerfsTer24(p.I194Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ANO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70105784:70105784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743C>T
AA Mutation	p.Thr248Met(p.T248M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355303
Start	70155965:70155965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480A>G
AA Mutation	p.Thr494Ala(p.T494A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355303
Start	70161707:70161707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1866C>A
Mutation Classification	Silent
Feature Type	Transcript