Colon Cancer: Gene >> EWSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29297895:29297895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Trp(p.R455W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29299604:29299604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1684G>A
AA Mutation	p.Asp562Asn(p.D562N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29299633:29299633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1713G>A
AA Mutation	p.Met571Ile(p.M571I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29299694:29299694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1774C>T
AA Mutation	p.Arg592Cys(p.R592C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29298754:29298754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439C>T
AA Mutation	p.Pro480Leu(p.P480L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29288737:29288737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Cys(p.R309C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397938
Start	29288664:29288664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397938
Start	29292162:29292162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397938
Start	29299780:29299780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397938
Start	29299777:29299777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1857G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397938
Start	29299672:29299672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148438243
CDS Mutation	c.1752C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397938
Start	29286992:29286992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397938
Start	29278048:29278048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.250delC
AA Mutation	p.Gln84ArgfsTer80(p.Q84Rfs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397938
Start	29299775:29299775(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1860delG
AA Mutation	p.Pro622LeufsTer4(p.P622Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397938
Start	29299840:29299840(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1924delA
AA Mutation	p.Met642TrpfsTer25(p.M642Wfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000397938
Start	29298798:29298798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483G>T
AA Mutation	p.Gly495Ter(p.G495*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397938
Start	29299731:29299732(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1812dupC
AA Mutation	p.Met605HisfsTer40(p.M605Hfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397938
Start	29299733:29299734(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1813_1814insCCTC
AA Mutation	p.Met605ThrfsTer41(p.M605Tfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EWSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29299798:29299798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1878G>A
AA Mutation	p.Met626Ile(p.M626I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397938
Start	29278180:29278180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377C>T
AA Mutation	p.Ala126Val(p.A126V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript