Colon Cancer: Gene >> DDX17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38488011:38488011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552G>A
AA Mutation	p.Ala518Thr(p.A518T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38494742:38494742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102G>A
AA Mutation	p.Glu368Lys(p.E368K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38494045:38494045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301T>C
AA Mutation	p.Leu434Pro(p.L434P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38486278:38486278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1847G>A
AA Mutation	p.Gly616Asp(p.G616D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38486380:38486380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745A>T
AA Mutation	p.Asp582Val(p.D582V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38501152:38501152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416C>T
AA Mutation	p.Pro139Leu(p.P139L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38493740:38493740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357A>G
AA Mutation	p.Ser453Gly(p.S453G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000403230
Start	38486163:38486163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1962A>C
AA Mutation	p.Glu654Asp(p.E654D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403230
Start	38485992:38485992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2133G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403230
Start	38506199:38506199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403230
Start	38506088:38506088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000403230
Start	38501206:38501206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759023106
CDS Mutation	c.362delA
AA Mutation	p.Lys121SerfsTer4(p.K121Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000403230
Start	38499400:38499400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>T
AA Mutation	p.Gln180Ter(p.Q180*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DDX17

No Mutation Annotation!