Colon Cancer: Gene >> QKI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563674:163563674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889G>A
AA Mutation	p.Ala297Thr(p.A297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563425:163563425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640C>T
AA Mutation	p.Leu214Phe(p.L214F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163535062:163535062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>T
AA Mutation	p.Gln161His(p.Q161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163566724:163566724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938C>T
AA Mutation	p.Ala313Val(p.A313V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163566742:163566742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777858938
CDS Mutation	c.956G>A
AA Mutation	p.Arg319Gln(p.R319Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163566775:163566775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779943694
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Lys(p.R330K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163455388:163455388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163562015:163562015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163415286:163415286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163563682:163563682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000361752
Start	163561988:163561988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>T
AA Mutation	p.Gly185Ter(p.G185*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000361752
Start	163455365:163455365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>T
AA Mutation	p.Gly77Ter(p.G77*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000361752
Start	163455410:163455410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>T
AA Mutation	p.Glu92Ter(p.E92*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361752
Start	163562071:163562071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> QKI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563510:163563510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142647102
CDS Mutation	c.725G>A
AA Mutation	p.Arg242His(p.R242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163566786:163566786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Ala334Thr(p.A334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163566725:163566725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765276688
CDS Mutation	c.939G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163455295:163455295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163535005:163535005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748022503
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript