Colon Cancer: Gene >> KNG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186741699:186741699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303A>C
AA Mutation	p.Lys435Gln(p.K435Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186741792:186741792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396G>A
AA Mutation	p.Glu466Lys(p.E466K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186731591:186731591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369801278
CDS Mutation	c.719G>A
AA Mutation	p.Arg240Gln(p.R240Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186741991:186741991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1595C>T
AA Mutation	p.Thr532Ile(p.T532I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186727251:186727251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579G>T
AA Mutation	p.Leu193Phe(p.L193F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186742098:186742098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702C>T
AA Mutation	p.Leu568Phe(p.L568F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186741813:186741813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1417C>T
AA Mutation	p.His473Tyr(p.H473Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265023
Start	186725225:186725225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529T>G
AA Mutation	p.Phe177Val(p.F177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265023
Start	186741791:186741791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779550579
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265023
Start	186742262:186742262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1866T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000265023
Start	186742293:186742293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897G>T
AA Mutation	p.Glu633Ter(p.E633*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000265023
Start	186741696:186741696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300G>T
AA Mutation	p.Glu434Ter(p.E434*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KNG1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265023
Start	186742223:186742223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763042709
CDS Mutation	c.1827G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265023
Start	186727266:186727266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265023
Start	186725233:186725233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000265023
Start	186742293:186742293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897G>T
AA Mutation	p.Glu633Ter(p.E633*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript