Colon Cancer: Gene >> ETV5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186105347:186105347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>T
AA Mutation	p.Pro64Ser(p.P64S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186066004:186066004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767684440
CDS Mutation	c.719G>A
AA Mutation	p.Arg240His(p.R240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186048721:186048721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451C>T
AA Mutation	p.Thr484Ile(p.T484I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186081088:186081088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320C>T
AA Mutation	p.Ala107Val(p.A107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186079913:186079913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554G>T
AA Mutation	p.Gly185Val(p.G185V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186057453:186057453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769924564
CDS Mutation	c.1009G>A
AA Mutation	p.Asp337Asn(p.D337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186052061:186052061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427His(p.R427H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186079892:186079892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779639231
CDS Mutation	c.575C>T
AA Mutation	p.Ala192Val(p.A192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186048658:186048658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514C>T
AA Mutation	p.Ala505Val(p.A505V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186048758:186048758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138683352
CDS Mutation	c.1414G>A
AA Mutation	p.Glu472Lys(p.E472K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186066045:186066045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186079852:186079852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186080077:186080077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186065904:186065904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139774137
CDS Mutation	c.819T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000306376
Start	186057191:186057191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093C>T
AA Mutation	p.Arg365Ter(p.R365*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000306376
Start	186052029:186052029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ETV5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186081170:186081170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238C>A
AA Mutation	p.Leu80Ile(p.L80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186048793:186048793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379C>T
AA Mutation	p.Pro460Leu(p.P460L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186065952:186065952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370362112
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186048828:186048828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186065838:186065838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306376
Start	186080012:186080012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.455delC
AA Mutation	p.Pro152HisfsTer55(p.P152Hfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript