Colon Cancer: Gene >> KIF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114096394:114096394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564040906
CDS Mutation	c.317G>A
AA Mutation	p.Arg106His(p.R106H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374118
Start	114093495:114093495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372317733
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114095039:114095039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527311501
CDS Mutation	c.689G>A
AA Mutation	p.Arg230Gln(p.R230Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114097345:114097345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188T>C
AA Mutation	p.Val63Ala(p.V63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114096077:114096077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>A
AA Mutation	p.Ser152Asn(p.S152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114092617:114092617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208G>A
AA Mutation	p.Gly403Asp(p.G403D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114096131:114096131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>C
AA Mutation	p.Ser134Thr(p.S134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114093964:114093964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908A>G
AA Mutation	p.Lys303Arg(p.K303R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114097352:114097352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Trp(p.R61W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374118
Start	114094253:114094253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827C>T
AA Mutation	p.Ala276Val(p.A276V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374118
Start	114092388:114092388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775468266
CDS Mutation	c.1347A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374118
Start	114091996:114091996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1407G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374118
Start	114096453:114096453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374118
Start	114092356:114092356(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1379delC
AA Mutation	p.Pro460ArgfsTer66(p.P460Rfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KIF12

No Mutation Annotation!