Colon Cancer: Gene >> TAB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30859534:30859534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Cys(p.R19C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30854634:30854634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031G>A
AA Mutation	p.Gly344Glu(p.G344E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30854454:30854454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763580207
CDS Mutation	c.1211C>T
AA Mutation	p.Thr404Met(p.T404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30854844:30854844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821A>G
AA Mutation	p.Asn274Ser(p.N274S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30831462:30831462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749567654
CDS Mutation	c.2104C>T
AA Mutation	p.Arg702Cys(p.R702C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30854922:30854922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777860992
CDS Mutation	c.743C>T
AA Mutation	p.Thr248Met(p.T248M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30852788:30852788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752852470
CDS Mutation	c.1700C>T
AA Mutation	p.Ala567Val(p.A567V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378933
Start	30854453:30854453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371431555
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378933
Start	30855368:30855368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378933
Start	30834106:30834106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378933
Start	30855206:30855206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378933
Start	30843017:30843017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1837delT
AA Mutation	p.Tyr613MetfsTer4(p.Y613Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378933
Start	30855394:30855394(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.271delC
AA Mutation	p.Gln91AsnfsTer27(p.Q91Nfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000378933
Start	30854284:30854284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Ter(p.R461*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000378933
Start	30854915:30854915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750G>A
AA Mutation	p.Trp250Ter(p.W250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30831519:30831519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2047G>A
AA Mutation	p.Glu683Lys(p.E683K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30846637:30846637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718A>G
AA Mutation	p.Glu573Gly(p.E573G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30854509:30854509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>T
AA Mutation	p.Pro386Ser(p.P386S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30846622:30846622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733G>T
AA Mutation	p.Arg578Ile(p.R578I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30854520:30854520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1145G>T
AA Mutation	p.Arg382Met(p.R382M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378933
Start	30859543:30859543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46C>A
AA Mutation	p.Leu16Ile(p.L16I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000378933
Start	30859540:30859540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770225305
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Ter(p.R17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript