Colon Cancer: Gene >> DTX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59181771:59181771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>A
AA Mutation	p.Asp82Asn(p.D82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59181988:59181988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372277661
CDS Mutation	c.461G>A
AA Mutation	p.Arg154His(p.R154H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59182156:59182156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629G>T
AA Mutation	p.Gly210Val(p.G210V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59182137:59182137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199568679
CDS Mutation	c.610G>A
AA Mutation	p.Val204Met(p.V204M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59192105:59192105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229C>T
AA Mutation	p.Thr410Ile(p.T410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59189245:59189245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376061897
CDS Mutation	c.1081G>A
AA Mutation	p.Val361Ile(p.V361I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59191119:59191119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165A>C
AA Mutation	p.Thr389Pro(p.T389P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59204760:59204760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376862310
CDS Mutation	c.1711G>A
AA Mutation	p.Val571Ile(p.V571I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000227451
Start	59182284:59182284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764119701
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227451
Start	59199719:59199719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780121144
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227451
Start	59181998:59181998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749542653
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227451
Start	59191136:59191136(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1188delA
AA Mutation	p.Lys396AsnfsTer34(p.K396Nfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227451
Start	59195354:59195354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772386010
CDS Mutation	c.1527delC
AA Mutation	p.Gly510AlafsTer35(p.G510Afs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000227451
Start	59192152:59192152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276C>T
AA Mutation	p.Gln426Ter(p.Q426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DTX4

No Mutation Annotation!