Colon Cancer: Gene >> KCMF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85028024:85028024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152C>A
AA Mutation	p.Pro51Gln(p.P51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85043657:85043657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418A>G
AA Mutation	p.Arg140Gly(p.R140G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85049464:85049464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>A
AA Mutation	p.Leu234Met(p.L234M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85027914:85027914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42A>C
AA Mutation	p.Lys14Asn(p.K14N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85046111:85046111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>T
AA Mutation	p.Ser145Leu(p.S145L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85043597:85043597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779570237
CDS Mutation	c.358G>A
AA Mutation	p.Asp120Asn(p.D120N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409785
Start	85035098:85035098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765616425
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409785
Start	85053196:85053196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409785
Start	85046193:85046193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409785
Start	85053400:85053400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCMF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85049434:85049434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770915691
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409785
Start	85046123:85046123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446G>A
AA Mutation	p.Arg149Gln(p.R149Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409785
Start	85035098:85035098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765616425
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript