Colon Cancer: Gene >> TBXAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	140007155:140007155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78666490
CDS Mutation	c.1199C>T
AA Mutation	p.Thr400Met(p.T400M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139953437:139953437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520G>A
AA Mutation	p.Asp174Asn(p.D174N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139953419:139953419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373695119
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139829406:139829406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16T>C
AA Mutation	p.Phe6Leu(p.F6L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139962042:139962042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Trp(p.R315W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	140017687:140017687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs5764
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Trp(p.R461W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139961922:139961922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761419784
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Trp(p.R275W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139955571:139955571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748558139
CDS Mutation	c.652G>A
AA Mutation	p.Glu218Lys(p.E218K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139955537:139955537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618G>T
AA Mutation	p.Glu206Asp(p.E206D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336425
Start	140007171:140007171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548305901
CDS Mutation	c.1215G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336425
Start	140017821:140017821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336425
Start	140015840:140015840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147299625
CDS Mutation	c.1344G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336425
Start	140020087:140020087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200481367
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336425
Start	140020075:140020075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1578C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336425
Start	139955522:139955522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575820680
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TBXAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139936213:139936213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356C>G
AA Mutation	p.Ser119Trp(p.S119W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139962193:139962193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094A>T
AA Mutation	p.Glu365Val(p.E365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	140017676:140017676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200831963
CDS Mutation	c.1370C>T
AA Mutation	p.Thr457Met(p.T457M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336425
Start	139953395:139953395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771992790
CDS Mutation	c.478G>A
AA Mutation	p.Asp160Asn(p.D160N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript