Colon Cancer: Gene >> EYA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133456606:133456606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>T
AA Mutation	p.Ala110Ser(p.A110S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133512930:133512930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393C>A
AA Mutation	p.Leu465Ile(p.L465I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133464844:133464844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790A>G
AA Mutation	p.Ser264Gly(p.S264G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133515380:133515380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1561C>A
AA Mutation	p.Leu521Met(p.L521M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133523109:133523109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670C>T
AA Mutation	p.Ala557Val(p.A557V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133446650:133446650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104T>C
AA Mutation	p.Leu35Pro(p.L35P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133462352:133462352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455T>C
AA Mutation	p.Leu152Pro(p.L152P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133506133:133506133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1219C>T
AA Mutation	p.Leu407Phe(p.L407F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133456628:133456628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350T>C
AA Mutation	p.Leu117Pro(p.L117P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133528733:133528733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848G>T
AA Mutation	p.Met616Ile(p.M616I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133462760:133462760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720G>T
AA Mutation	p.Met240Ile(p.M240I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133506150:133506150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236G>T
AA Mutation	p.Met412Ile(p.M412I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367895
Start	133515434:133515434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1615A>G
AA Mutation	p.Arg539Gly(p.R539G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133506137:133506137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760787542
CDS Mutation	c.1223G>A
AA Mutation	p.Arg408His(p.R408H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133468648:133468648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755455584
CDS Mutation	c.887C>T
AA Mutation	p.Ser296Leu(p.S296L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367895
Start	133456584:133456584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367895
Start	133462718:133462718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367895
Start	133468664:133468664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EYA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133446737:133446737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191C>A
AA Mutation	p.Thr64Asn(p.T64N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133382397:133382397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39G>T
AA Mutation	p.Lys13Asn(p.K13N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133515388:133515388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1569T>G
AA Mutation	p.Asp523Glu(p.D523E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367895
Start	133523109:133523109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670C>T
AA Mutation	p.Ala557Val(p.A557V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367895
Start	133462425:133462425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199701258
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367895
Start	133481545:133481545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367895
Start	133483064:133483064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000367895
Start	133506145:133506145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231G>T
AA Mutation	p.Glu411Ter(p.E411*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript