Colon Cancer: Gene >> AMER2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169734:25169734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886C>T
AA Mutation	p.Pro629Leu(p.P629L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169799:25169799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1821G>T
AA Mutation	p.Lys607Asn(p.K607N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171522:25171522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98G>A
AA Mutation	p.Gly33Glu(p.G33E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171328:25171328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292A>G
AA Mutation	p.Thr98Ala(p.T98A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171268:25171268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352G>A
AA Mutation	p.Gly118Ser(p.G118S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169935:25169935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201439289
CDS Mutation	c.1685C>T
AA Mutation	p.Pro562Leu(p.P562L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170452:25170452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1168G>A
AA Mutation	p.Glu390Lys(p.E390K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170209:25170209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411G>A
AA Mutation	p.Glu471Lys(p.E471K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169680:25169680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940G>A
AA Mutation	p.Arg647His(p.R647H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170323:25170323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297G>A
AA Mutation	p.Asp433Asn(p.D433N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25169830:25169830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790G>A
AA Mutation	p.Arg597Gln(p.R597Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170193:25170193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427C>A
AA Mutation	p.Thr476Asn(p.T476N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25170633:25170633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537405504
CDS Mutation	c.987G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25169958:25169958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1662G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171248:25171248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25170009:25170009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25170231:25170231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171335:25171335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000515384
Start	25171344:25171344(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.276delG
AA Mutation	p.Ser94AlafsTer8(p.S94Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000515384
Start	25170392:25170392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228A>T
AA Mutation	p.Lys410Ter(p.K410*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AMER2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25171046:25171046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Trp(p.R192W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000515384
Start	25170598:25170598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171326:25171326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515384
Start	25171446:25171446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript