Colon Cancer: Gene >> HMGXB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150037515:150037515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3139G>C
AA Mutation	p.Asp1047His(p.D1047H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150045533:150045533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3536C>T
AA Mutation	p.Thr1179Ile(p.T1179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150024401:150024401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188995699
CDS Mutation	c.1919C>T
AA Mutation	p.Ser640Leu(p.S640L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150004859:150004859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187156146
CDS Mutation	c.745G>A
AA Mutation	p.Ala249Thr(p.A249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150045590:150045590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183054657
CDS Mutation	c.3593C>T
AA Mutation	p.Ala1198Val(p.A1198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150026831:150026831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565914929
CDS Mutation	c.2324G>A
AA Mutation	p.Arg775Gln(p.R775Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150036858:150036858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2944A>C
AA Mutation	p.Thr982Pro(p.T982P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150036828:150036828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753841260
CDS Mutation	c.2914G>A
AA Mutation	p.Val972Met(p.V972M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150052116:150052116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4541G>T
AA Mutation	p.Arg1514Leu(p.R1514L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150047693:150047693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3758G>A
AA Mutation	p.Ser1253Asn(p.S1253N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150004983:150004983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869A>C
AA Mutation	p.Lys290Thr(p.K290T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150050399:150050399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4087C>G
AA Mutation	p.Leu1363Val(p.L1363V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000613459
Start	150006587:150006587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000613459
Start	150041963:150041963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000613459
Start	150045525:150045525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3528G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HMGXB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150041856:150041856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3355T>G
AA Mutation	p.Cys1119Gly(p.C1119G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000613459
Start	150018584:150018584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1666C>T
AA Mutation	p.Arg556Trp(p.R556W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000613459
Start	150041855:150041855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3354G>A
Mutation Classification	Silent
Feature Type	Transcript