Colon Cancer: Gene >> RUNDC3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87628926:87628926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103A>G
AA Mutation	p.Asn35Asp(p.N35D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87807402:87807402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>T
AA Mutation	p.Ser346Leu(p.S346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87777889:87777889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Ser314Phe(p.S314F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000338056
Start	87770749:87770749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849G>T
AA Mutation	p.Lys283Asn(p.K283N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87741510:87741510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>C
AA Mutation	p.Lys204Thr(p.K204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87816211:87816211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557040251
CDS Mutation	c.1225C>A
AA Mutation	p.Gln409Lys(p.Q409K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87807495:87807495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769895514
CDS Mutation	c.1130G>A
AA Mutation	p.Arg377Gln(p.R377Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338056
Start	87829931:87829931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746431545
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338056
Start	87710596:87710596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338056
Start	87700521:87700521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338056
Start	87650834:87650834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338056
Start	87628841:87628841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.23delG
AA Mutation	p.Gly8AlafsTer2(p.G8Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000338056
Start	87777810:87777810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862G>T
AA Mutation	p.Glu288Ter(p.E288*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000338056
Start	87777825:87777825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Ter(p.R293*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000338056
Start	87700420:87700420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RUNDC3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87777820:87777820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872G>T
AA Mutation	p.Arg291Leu(p.R291L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338056
Start	87816246:87816246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260A>C
AA Mutation	p.Leu420Phe(p.L420F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338056
Start	87770638:87770638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141708572
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript