Colon Cancer: Gene >> KRT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52649951:52649951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824G>A
AA Mutation	p.Arg275His(p.R275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52650439:52650439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371361222
CDS Mutation	c.700G>A
AA Mutation	p.Asp234Asn(p.D234N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52646750:52646750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852629
CDS Mutation	c.1459G>A
AA Mutation	p.Glu487Lys(p.E487K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52650436:52650436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703A>G
AA Mutation	p.Ser235Gly(p.S235G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52645167:52645167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772C>A
AA Mutation	p.Ser591Tyr(p.S591Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52646777:52646777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144860513
CDS Mutation	c.1432G>A
AA Mutation	p.Ala478Thr(p.A478T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52649045:52649045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.919A>G
AA Mutation	p.Asn307Asp(p.N307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52645354:52645354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530945813
CDS Mutation	c.1585G>A
AA Mutation	p.Gly529Arg(p.G529R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52651779:52651779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530180060
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Cys(p.R122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309680
Start	52648314:52648314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556683411
CDS Mutation	c.981T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309680
Start	52647752:52647753(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1225dupG
AA Mutation	p.Glu409GlyfsTer10(p.E409Gfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KRT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52647773:52647773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1205T>C
AA Mutation	p.Val402Ala(p.V402A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309680
Start	52650426:52650426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713G>T
AA Mutation	p.Arg238Ile(p.R238I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309680
Start	52646835:52646835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1374G>A
Mutation Classification	Silent
Feature Type	Transcript