Colon Cancer: Gene >> KRT17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41620831:41620831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143477910
CDS Mutation	c.1009G>A
AA Mutation	p.Val337Met(p.V337M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41619599:41619599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369304694
CDS Mutation	c.1294C>T
AA Mutation	p.Arg432Cys(p.R432C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41624161:41624161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375507162
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41624262:41624262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248G>T
AA Mutation	p.Gly83Val(p.G83V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41622959:41622959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506T>C
AA Mutation	p.Phe169Ser(p.F169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41622464:41622464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563A>G
AA Mutation	p.Asn188Ser(p.N188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41622489:41622489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780251083
CDS Mutation	c.538C>T
AA Mutation	p.Arg180Cys(p.R180C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311208
Start	41621023:41621023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148958331
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311208
Start	41624445:41624445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753167272
CDS Mutation	c.65delG
AA Mutation	p.Gly22AlafsTer93(p.G22Afs*93)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000311208
Start	41620535:41620535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753628412
CDS Mutation	c.1204+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KRT17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41620687:41620687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368177544
CDS Mutation	c.1153C>T
AA Mutation	p.Arg385Cys(p.R385C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41620841:41620841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999C>A
AA Mutation	p.Asn333Lys(p.N333K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311208
Start	41620991:41620991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935T>A
AA Mutation	p.Ile312Lys(p.I312K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript