Colon Cancer: Gene >> MTUS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754718:17754718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>T
AA Mutation	p.Val364Leu(p.V364L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17653269:17653269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3301G>T
AA Mutation	p.Asp1101Tyr(p.D1101Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754135:17754135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1673G>T
AA Mutation	p.Arg558Ile(p.R558I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754121:17754121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1687G>A
AA Mutation	p.Ala563Thr(p.A563T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754308:17754308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1500A>G
AA Mutation	p.Ile500Met(p.I500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755065:17755065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747545946
CDS Mutation	c.743A>G
AA Mutation	p.Asp248Gly(p.D248G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755156:17755156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373564089
CDS Mutation	c.652G>A
AA Mutation	p.Ala218Thr(p.A218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755075:17755075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>A
AA Mutation	p.Ala245Thr(p.A245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754901:17754901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907A>G
AA Mutation	p.Asn303Asp(p.N303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754238:17754238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1570G>T
AA Mutation	p.Asp524Tyr(p.D524Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754975:17754975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833G>A
AA Mutation	p.Gly278Glu(p.G278E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17754467:17754467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761790276
CDS Mutation	c.1341G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17755160:17755160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760600748
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17715828:17715828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2523C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17754866:17754866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17743632:17743632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2259T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17754764:17754764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17754110:17754110(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1698delA
AA Mutation	p.Ala567GlnfsTer4(p.A567Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17754908:17754908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.900delA
AA Mutation	p.Val301SerfsTer37(p.V301Sfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17646059:17646059(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3680delA
AA Mutation	p.Asn1227ThrfsTer58(p.N1227Tfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000262102
Start	17755150:17755150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658G>T
AA Mutation	p.Glu220Ter(p.E220*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000262102
Start	17684498:17684499(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2667_2668insGTATTA
AA Mutation	p.Gln889_Pro890insValLeu(p.Q889_P890insVL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTUS1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262102
Start	17715901:17715901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2450C>A
AA Mutation	p.Ser817Tyr(p.S817Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17653479:17653479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3234A>C
AA Mutation	p.Glu1078Asp(p.E1078D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17715846:17715846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2505G>T
AA Mutation	p.Gln835His(p.Q835H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754499:17754499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309A>C
AA Mutation	p.Lys437Gln(p.K437Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755596:17755596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212C>A
AA Mutation	p.Ser71Tyr(p.S71Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17653219:17653219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3351A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17753984:17753984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17723812:17723813(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2308dupA
AA Mutation	p.Thr770AsnfsTer11(p.T770Nfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript