Colon Cancer: Gene >> AMIGO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078245:47078245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758A>G
AA Mutation	p.Asp253Gly(p.D253G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078104:47078104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>T
AA Mutation	p.Ala300Val(p.A300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47077710:47077710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293G>T
AA Mutation	p.Gln431His(p.Q431H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47077460:47077460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543G>C
AA Mutation	p.Asp515His(p.D515H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078414:47078414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589T>G
AA Mutation	p.Leu197Val(p.L197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078861:47078861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142G>A
AA Mutation	p.Ala48Thr(p.A48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078395:47078395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>A
AA Mutation	p.Arg203Gln(p.R203Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078702:47078702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Cys(p.R101C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078687:47078687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316A>G
AA Mutation	p.Thr106Ala(p.T106A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266581
Start	47077458:47077458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266581
Start	47077872:47077872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774547090
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266581
Start	47077674:47077674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778696499
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266581
Start	47078602:47078602(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.401delA
AA Mutation	p.Asn134MetfsTer7(p.N134Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AMIGO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078222:47078222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372100851
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266581
Start	47078633:47078633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370T>G
AA Mutation	p.Leu124Val(p.L124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266581
Start	47077773:47077773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753773906
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266581
Start	47078097:47078097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266581
Start	47077674:47077674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778696499
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript