Colon Cancer: Gene >> KRT82

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52400068:52400068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61730589
CDS Mutation	c.859G>A
AA Mutation	p.Gly287Ser(p.G287S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52396923:52396923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028T>C
AA Mutation	p.Ile343Thr(p.I343T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52396181:52396181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120G>C
AA Mutation	p.Ala374Pro(p.A374P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52403818:52403818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503T>C
AA Mutation	p.Ile168Thr(p.I168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52396046:52396046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255A>G
AA Mutation	p.Thr419Ala(p.T419A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52401326:52401326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374377608
CDS Mutation	c.644G>A
AA Mutation	p.Arg215His(p.R215H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52405884:52405884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149651491
CDS Mutation	c.394G>A
AA Mutation	p.Ala132Thr(p.A132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52400074:52400074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529536223
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52406201:52406201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185048433
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52401327:52401327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368818089
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Cys(p.R215C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52400046:52400046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199503440
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257974
Start	52406101:52406101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199864780
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257974
Start	52395095:52395095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257974
Start	52394990:52394990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1527delC
AA Mutation	p.Ser510AlafsTer52(p.S510Afs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT82

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257974
Start	52403768:52403768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750740979
CDS Mutation	c.553G>A
AA Mutation	p.Gly185Arg(p.G185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257974
Start	52403814:52403814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript