Colon Cancer: Gene >> TSGA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99078671:99078671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870T>G
AA Mutation	p.Ser290Arg(p.S290R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355053
Start	99068889:99068889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1217A>C
AA Mutation	p.Glu406Ala(p.E406A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99071821:99071821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992G>A
AA Mutation	p.Arg331Gln(p.R331Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99081377:99081377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632A>G
AA Mutation	p.Glu211Gly(p.E211G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99109432:99109432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201271167
CDS Mutation	c.8G>A
AA Mutation	p.Arg3Gln(p.R3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99071825:99071825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758866582
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Cys(p.R330C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99035252:99035252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1592C>T
AA Mutation	p.Ala531Val(p.A531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99020318:99020318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1779G>C
AA Mutation	p.Gln593His(p.Q593H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99109403:99109403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37T>C
AA Mutation	p.Ser13Pro(p.S13P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99035359:99035359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485G>T
AA Mutation	p.Gln495His(p.Q495H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355053
Start	99020481:99020481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778622550
CDS Mutation	c.1616G>T
AA Mutation	p.Arg539Met(p.R539M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99109419:99109419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21A>C
AA Mutation	p.Lys7Asn(p.K7N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99065106:99065106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237A>C
AA Mutation	p.Met413Leu(p.M413L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355053
Start	99109427:99109427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355053
Start	99078701:99078701(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.840delA
AA Mutation	p.Lys280AsnfsTer14(p.K280Nfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000355053
Start	99108940:99108940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>T
AA Mutation	p.Glu35Ter(p.E35*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000355053
Start	99109433:99109433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7C>T
AA Mutation	p.Arg3Ter(p.R3*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000355053
Start	99035228:99035228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1614+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TSGA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99020448:99020448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1649T>C
AA Mutation	p.Ile550Thr(p.I550T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355053
Start	99018287:99018287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1985C>A
AA Mutation	p.Ser662Tyr(p.S662Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript