Colon Cancer: Gene >> MOV10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112694553:112694553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755646925
CDS Mutation	c.1396C>T
AA Mutation	p.Arg466Cys(p.R466C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112692773:112692773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>T
AA Mutation	p.Glu328Asp(p.E328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112700449:112700449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201257888
CDS Mutation	c.2954G>A
AA Mutation	p.Arg985Gln(p.R985Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112689966:112689966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704C>T
AA Mutation	p.Ala235Val(p.A235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112690071:112690071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Gln(p.R270Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112692811:112692811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4448516
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112698468:112698468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2498A>G
AA Mutation	p.Tyr833Cys(p.Y833C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112698074:112698074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2279G>A
AA Mutation	p.Arg760Gln(p.R760Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112696166:112696166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765842366
CDS Mutation	c.1798G>A
AA Mutation	p.Ala600Thr(p.A600T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112699722:112699722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2621G>A
AA Mutation	p.Ser874Asn(p.S874N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112695458:112695458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663C>G
AA Mutation	p.Pro555Ala(p.P555A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112692813:112692813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112689127:112689127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112692767:112692767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112696500:112696500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357443
Start	112691740:112691740(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.915delC
AA Mutation	p.Met306CysfsTer26(p.M306Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000357443
Start	112696216:112696216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848C>A
AA Mutation	p.Tyr616Ter(p.Y616*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000357443
Start	112689138:112689139(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.341+11_341+12dupGT
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MOV10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357443
Start	112698094:112698094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2299G>A
AA Mutation	p.Ala767Thr(p.A767T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112691788:112691788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372753999
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112692923:112692923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114735246
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112694806:112694806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1530T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357443
Start	112698460:112698460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2490C>T
Mutation Classification	Silent
Feature Type	Transcript