Colon Cancer: Gene >> KRT20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000167588
Start	40878250:40878250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034A>G
AA Mutation	p.Asn345Ser(p.N345S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000167588
Start	40876426:40876426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371817674
CDS Mutation	c.1210G>A
AA Mutation	p.Val404Met(p.V404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000167588
Start	40880249:40880249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643C>A
AA Mutation	p.Leu215Ile(p.L215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000167588
Start	40878294:40878294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759321465
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000167588
Start	40880623:40880623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KRT20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000167588
Start	40878199:40878199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748744256
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362Gln(p.R362Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000167588
Start	40884803:40884803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383G>A
AA Mutation	p.Arg128Gln(p.R128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000167588
Start	40884940:40884940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753053653
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript