Colon Cancer: Gene >> EYA2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327619
Start	47001473:47001473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155G>T
AA Mutation	p.Arg52Ile(p.R52I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47016240:47016240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Gly120Cys(p.G120C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47074305:47074305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142696386
CDS Mutation	c.631G>A
AA Mutation	p.Val211Ile(p.V211I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47169155:47169155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.995A>G
AA Mutation	p.His332Arg(p.H332R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47072232:47072232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141379321
CDS Mutation	c.463G>A
AA Mutation	p.Gly155Ser(p.G155S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47183329:47183329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474G>A
AA Mutation	p.Gly492Ser(p.G492S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47005016:47005016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230G>C
AA Mutation	p.Gly77Ala(p.G77A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47188118:47188118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>C
AA Mutation	p.Glu534Asp(p.E534D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47097124:47097124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844T>G
AA Mutation	p.Phe282Val(p.F282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47172776:47172776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201557595
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47143067:47143067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47172782:47172782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200642511
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47074184:47074184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47172785:47172785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148023070
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47097093:47097093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778431393
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EYA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47004988:47004988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>T
AA Mutation	p.Ala68Ser(p.A68S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47005016:47005016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230G>C
AA Mutation	p.Gly77Ala(p.G77A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327619
Start	47143077:47143077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368297287
CDS Mutation	c.907C>T
AA Mutation	p.Arg303Cys(p.R303C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47172788:47172788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1119C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327619
Start	47089300:47089300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript