Colon Cancer: Gene >> DHX35

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000252011
Start	38972559:38972559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175C>T
AA Mutation	p.Leu59Phe(p.L59F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000252011
Start	38994879:38994879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641A>G
AA Mutation	p.Asp214Gly(p.D214G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	39010328:39010328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143299906
CDS Mutation	c.1271G>A
AA Mutation	p.Arg424His(p.R424H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	39023753:39023753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1657G>A
AA Mutation	p.Glu553Lys(p.E553K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	39006326:39006326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138301896
CDS Mutation	c.1192C>T
AA Mutation	p.Arg398Cys(p.R398C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	39030763:39030763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1943A>G
AA Mutation	p.Lys648Arg(p.K648R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	39010339:39010339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>A
AA Mutation	p.Ala428Thr(p.A428T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	39034262:39034262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012C>T
AA Mutation	p.Ala671Val(p.A671V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252011
Start	39021932:39021932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141540547
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252011
Start	39021875:39021875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534416816
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252011
Start	39006238:39006238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252011
Start	39021854:39021854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252011
Start	39025343:39025343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1785C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000252011
Start	39034267:39034267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017G>T
AA Mutation	p.Glu673Ter(p.E673*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000252011
Start	39023693:39023693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597C>T
AA Mutation	p.Arg533Ter(p.R533*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DHX35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252011
Start	38969125:38969125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>G
AA Mutation	p.Leu29Val(p.L29V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000252011
Start	39003758:39003758(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