Colon Cancer: Gene >> KRT83

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293670
Start	52321152:52321152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Gly62Ser(p.G62S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293670
Start	52321131:52321131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776341669
CDS Mutation	c.205G>A
AA Mutation	p.Gly69Ser(p.G69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293670
Start	52316866:52316866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775630317
CDS Mutation	c.908G>A
AA Mutation	p.Arg303His(p.R303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293670
Start	52319285:52319285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464A>G
AA Mutation	p.Asn155Ser(p.N155S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293670
Start	52316891:52316891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766710639
CDS Mutation	c.883C>T
AA Mutation	p.Arg295Trp(p.R295W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000293670
Start	52316544:52316544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758485277
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293670
Start	52314724:52314724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293670
Start	52316021:52316021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148519033
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293670
Start	52317687:52317687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761449359
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293670
Start	52316561:52316561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748796258
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293670
Start	52321027:52321027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752860418
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KRT83

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293670
Start	52316997:52316997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293670
Start	52321115:52321115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.221delG
AA Mutation	p.Gly74AlafsTer27(p.G74Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript