Colon Cancer: Gene >> TNS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53061211:53061211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3305G>A
AA Mutation	p.Ser1102Asn(p.S1102N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53063374:53063374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749781369
CDS Mutation	c.4018G>A
AA Mutation	p.Val1340Met(p.V1340M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53057027:53057027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776T>G
AA Mutation	p.Leu259Arg(p.L259R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53051873:53051873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94C>T
AA Mutation	p.His32Tyr(p.H32Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53059214:53059214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573G>A
AA Mutation	p.Ala525Thr(p.A525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53062665:53062665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3791G>A
AA Mutation	p.Ser1264Asn(p.S1264N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53059361:53059361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553001534
CDS Mutation	c.1720G>A
AA Mutation	p.Gly574Arg(p.G574R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53058094:53058094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140911911
CDS Mutation	c.1087G>A
AA Mutation	p.Asp363Asn(p.D363N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53058605:53058605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1259T>G
AA Mutation	p.Phe420Cys(p.F420C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53059829:53059829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371331910
CDS Mutation	c.2188C>T
AA Mutation	p.Arg730Trp(p.R730W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53060683:53060683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533324165
CDS Mutation	c.2777G>A
AA Mutation	p.Arg926Gln(p.R926Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53055647:53055647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653G>T
AA Mutation	p.Trp218Leu(p.W218L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314250
Start	53052468:53052468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370897636
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314250
Start	53062437:53062437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314250
Start	53059720:53059720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773974809
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314250
Start	53053787:53053787(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.278delC
AA Mutation	p.Pro93GlnfsTer5(p.P93Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314250
Start	53059615:53059615(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1977delG
AA Mutation	p.Lys660AsnfsTer96(p.K660Nfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314250
Start	53059119:53059119(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1484delC
AA Mutation	p.Pro495ArgfsTer25(p.P495Rfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314250
Start	53058087:53058088(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1083dupA
AA Mutation	p.Gly362ArgfsTer43(p.G362Rfs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314250
Start	53058353:53058353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770007326
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378Gln(p.R378Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314250
Start	53061182:53061182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3276G>A
Mutation Classification	Silent
Feature Type	Transcript