Colon Cancer: Gene >> ETV4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319349
Start	43532814:43532814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>T
AA Mutation	p.Ser224Ile(p.S224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319349
Start	43528623:43528623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768121396
CDS Mutation	c.1351G>A
AA Mutation	p.Glu451Lys(p.E451K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319349
Start	43529141:43529141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224G>A
AA Mutation	p.Met408Ile(p.M408I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319349
Start	43533910:43533910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332G>A
AA Mutation	p.Ser111Asn(p.S111N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319349
Start	43532825:43532825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319349
Start	43529605:43529605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319349
Start	43530117:43530117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319349
Start	43529927:43529927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319349
Start	43533333:43533333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.399delC
AA Mutation	p.Arg134AspfsTer30(p.R134Dfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ETV4

No Mutation Annotation!