Colon Cancer: Gene >> CLSTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9731219:9731219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2735T>C
AA Mutation	p.Val912Ala(p.V912A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9735908:9735908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201640412
CDS Mutation	c.1711G>A
AA Mutation	p.Glu571Lys(p.E571K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9741229:9741229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384G>C
AA Mutation	p.Val462Leu(p.V462L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9730609:9730609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2845G>A
AA Mutation	p.Glu949Lys(p.E949K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9731304:9731304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757264934
CDS Mutation	c.2650G>A
AA Mutation	p.Ala884Thr(p.A884T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9743964:9743964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375187320
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Trp(p.R426W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9737534:9737534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540G>T
AA Mutation	p.Asp514Tyr(p.D514Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9773329:9773329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157G>A
AA Mutation	p.Val53Met(p.V53M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9741147:9741147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375763180
CDS Mutation	c.1466C>T
AA Mutation	p.Pro489Leu(p.P489L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9733501:9733501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327G>T
AA Mutation	p.Arg776Leu(p.R776L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9731764:9731764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754287069
CDS Mutation	c.2560G>A
AA Mutation	p.Ala854Thr(p.A854T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9751656:9751656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767264166
CDS Mutation	c.466G>A
AA Mutation	p.Asp156Asn(p.D156N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377298
Start	9731388:9731388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751722195
CDS Mutation	c.2566G>A
AA Mutation	p.Val856Ile(p.V856I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9733415:9733415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769167202
CDS Mutation	c.2413G>A
AA Mutation	p.Glu805Lys(p.E805K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9735561:9735561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789G>A
AA Mutation	p.Glu597Lys(p.E597K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9733495:9733495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781337343
CDS Mutation	c.2333G>A
AA Mutation	p.Arg778Gln(p.R778Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9735080:9735080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560870976
CDS Mutation	c.1978G>A
AA Mutation	p.Val660Ile(p.V660I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377298
Start	9749504:9749504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183348898
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377298
Start	9735565:9735565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768921068
CDS Mutation	c.1785C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377298
Start	9731380:9731380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2574C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377298
Start	9731861:9731861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745837689
CDS Mutation	c.2463C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377298
Start	9773313:9773313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.173delC
AA Mutation	p.Pro58HisfsTer2(p.P58Hfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377298
Start	9749901:9749901(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.662delA
AA Mutation	p.Asn221ThrfsTer5(p.N221Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000377298
Start	9749768:9749768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775304743
CDS Mutation	c.795G>A
AA Mutation	p.Trp265Ter(p.W265*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000377298
Start	9773375:9773375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111G>A
AA Mutation	p.Trp37Ter(p.W37*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000377298
Start	9736013:9736013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606C>T
AA Mutation	p.Arg536Ter(p.R536*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377298
Start	9735138:9735139(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1919dupC
AA Mutation	p.Val641GlyfsTer29(p.V641Gfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CLSTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377298
Start	9735509:9735509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1841C>A
AA Mutation	p.Pro614His(p.P614H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript