Colon Cancer: Gene >> STK25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241499271:241499271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Ala191Thr(p.A191T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241496444:241496444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>A
AA Mutation	p.Gly399Ser(p.G399S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241499295:241499295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.547G>A
AA Mutation	p.Ala183Thr(p.A183T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241498288:241498288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979C>T
AA Mutation	p.Pro327Ser(p.P327S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316586
Start	241498783:241498783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Gln(p.R258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241498650:241498650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>T
AA Mutation	p.Glu302Asp(p.E302D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241501665:241501665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200593123
CDS Mutation	c.74G>A
AA Mutation	p.Arg25His(p.R25H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241499060:241499060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700A>G
AA Mutation	p.Thr234Ala(p.T234A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241501685:241501685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241500227:241500227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241499317:241499317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777602273
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241498704:241498704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241496418:241496418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780044217
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241496508:241496508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772987757
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316586
Start	241499022:241499022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750489895
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STK25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316586
Start	241498333:241498333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749514218
CDS Mutation	c.934G>A
AA Mutation	p.Asp312Asn(p.D312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript