Colon Cancer: Gene >> TUSC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15748438:15748438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748401651
CDS Mutation	c.1001G>A
AA Mutation	p.Arg334His(p.R334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623186:15623186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>A
AA Mutation	p.Arg82Gln(p.R82Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15662189:15662189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601A>G
AA Mutation	p.Thr201Ala(p.T201A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000503731
Start	15748465:15748465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028G>T
AA Mutation	p.Ser343Ile(p.S343I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623137:15623137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196T>G
AA Mutation	p.Phe66Val(p.F66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15540459:15540459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>A
AA Mutation	p.Arg10His(p.R10H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15662272:15662272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684G>T
AA Mutation	p.Lys228Asn(p.K228N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15659511:15659511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368421691
CDS Mutation	c.431A>G
AA Mutation	p.Asn144Ser(p.N144S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623230:15623230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755902777
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Trp(p.R97W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15730680:15730680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15659638:15659638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15650727:15650727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755181425
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15540490:15540490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15673794:15673794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15748397:15748397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant;start_lost
Transcription ID	ENST00000503731
Start	15540433:15540433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7delG
AA Mutation	p.Ala3ProfsTer47(p.A3Pfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TUSC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15659589:15659589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756937528
CDS Mutation	c.509G>T
AA Mutation	p.Arg170Ile(p.R170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15540473:15540473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>T
AA Mutation	p.Arg15Trp(p.R15W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15659556:15659556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476G>A
AA Mutation	p.Arg159Lys(p.R159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623188:15623188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247A>C
AA Mutation	p.Asn83His(p.N83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript