Colon Cancer: Gene >> NKRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119590064:119590064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767690358
CDS Mutation	c.1361C>T
AA Mutation	p.Thr454Met(p.T454M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119590037:119590037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463Gln(p.R463Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119590941:119590941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484T>A
AA Mutation	p.Phe162Ile(p.F162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119590725:119590725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700A>C
AA Mutation	p.Lys234Gln(p.K234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119592485:119592485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13C>A
AA Mutation	p.Leu5Ile(p.L5I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304449
Start	119591266:119591266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304449
Start	119590576:119590576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304449
Start	119589435:119589435(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1990delA
AA Mutation	p.Arg664AspfsTer7(p.R664Dfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NKRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119589921:119589921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1504G>A
AA Mutation	p.Glu502Lys(p.E502K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304449
Start	119590892:119590892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144370117
CDS Mutation	c.533C>T
AA Mutation	p.Thr178Met(p.T178M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript