Colon Cancer: Gene >> KRT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52677138:52677138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175G>T
AA Mutation	p.Arg392Ile(p.R392I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52677725:52677725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888G>T
AA Mutation	p.Met296Ile(p.M296I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52675555:52675555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573T>C
AA Mutation	p.Tyr525His(p.Y525H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52678571:52678571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756537688
CDS Mutation	c.777G>A
AA Mutation	p.Met259Ile(p.M259I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52680264:52680264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201494492
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Cys(p.R29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52680083:52680083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266G>C
AA Mutation	p.Gly89Ala(p.G89A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52677124:52677124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189G>A
AA Mutation	p.Glu397Lys(p.E397K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52676363:52676363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757504428
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52675204:52675204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1924G>A
AA Mutation	p.Val642Ile(p.V642I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52678672:52678672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.676A>C
AA Mutation	p.Asn226His(p.N226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52679835:52679835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>A
AA Mutation	p.Glu172Lys(p.E172K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52676450:52676450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300G>A
AA Mutation	p.Glu434Lys(p.E434K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52680341:52680341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775323304
CDS Mutation	c.8G>A
AA Mutation	p.Arg3Gln(p.R3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52675415:52675415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1713C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52675310:52675310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52675559:52675559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52680250:52680250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52675208:52675208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1920C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52675526:52675526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545434207
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000252244
Start	52680017:52680031(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs527241748
CDS Mutation	c.318_332delTGGTGGCTTTGGTGG
AA Mutation	p.Phe109_Gly113del(p.F109_G113del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252244
Start	52678187:52678187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.843G>T
AA Mutation	p.Glu281Asp(p.E281D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252244
Start	52677077:52677077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137978741
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript