Colon Cancer: Gene >> TAF4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26227121:26227121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188G>A
AA Mutation	p.Arg63Gln(p.R63Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26286275:26286275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577643770
CDS Mutation	c.1366G>C
AA Mutation	p.Val456Leu(p.V456L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26315387:26315387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1991T>G
AA Mutation	p.Ile664Ser(p.I664S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26286189:26286189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280G>A
AA Mutation	p.Gly427Glu(p.G427E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000269142
Start	26274823:26274823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202073070
CDS Mutation	c.758C>T
AA Mutation	p.Pro253Leu(p.P253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26293492:26293492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793A>G
AA Mutation	p.Gln598Arg(p.Q598R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26274741:26274741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.676A>C
AA Mutation	p.Ser226Arg(p.S226R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26292325:26292325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670G>A
AA Mutation	p.Cys557Tyr(p.C557Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269142
Start	26275029:26275029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000269142
Start	26390011:26390011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2588G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269142
Start	26265201:26265201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765439658
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269142
Start	26286151:26286151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269142
Start	26321149:26321149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2082C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269142
Start	26293466:26293467(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1768_1769delCT
AA Mutation	p.Leu590ValfsTer11(p.L590Vfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000269142
Start	26285936:26285936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
AA Mutation	p.Gln343Ter(p.Q343*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000269142
Start	26315228:26315228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1833-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000269142
Start	26321057:26321073(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2003-13_2006delTCTGCTTCTGCAGGTAA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TAF4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26286474:26286474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1565C>T
AA Mutation	p.Pro522Leu(p.P522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26227074:26227074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>T
AA Mutation	p.Lys47Asn(p.K47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269142
Start	26357771:26357771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398A>G
AA Mutation	p.Arg800Gly(p.R800G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript