Colon Cancer: Gene >> STK24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98463764:98463764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>A
AA Mutation	p.Glu298Lys(p.E298K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98475303:98475303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422T>C
AA Mutation	p.Leu141Pro(p.L141P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98482276:98482276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367740523
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98474961:98474961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493T>C
AA Mutation	p.Ser165Pro(p.S165P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98466414:98466414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Glu261Lys(p.E261K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98460430:98460430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539699022
CDS Mutation	c.1100T>C
AA Mutation	p.Ile367Thr(p.I367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376547
Start	98475293:98475293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376547
Start	98466400:98466400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000376547
Start	98475310:98475310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>T
AA Mutation	p.Glu139Ter(p.E139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376547
Start	98461870:98461871(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758627015
CDS Mutation	c.992dupG
AA Mutation	p.Ser332GlnfsTer2(p.S332Qfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> STK24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376547
Start	98463783:98463783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>T
AA Mutation	p.Lys291Asn(p.K291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000376547
Start	98461896:98461896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.967G>T
AA Mutation	p.Glu323Ter(p.E323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript