Colon Cancer: Gene >> KIF2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62385496:62385496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2048C>A
AA Mutation	p.Ser683Tyr(p.S683Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62362453:62362453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344Gln(p.R344Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62363841:62363841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1409C>T
AA Mutation	p.Ala470Val(p.A470V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62350073:62350073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287G>A
AA Mutation	p.Arg96Gln(p.R96Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62355181:62355181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581A>T
AA Mutation	p.Asn194Ile(p.N194I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62363733:62363733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434Gln(p.R434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401507
Start	62373762:62373762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1722T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000401507
Start	62381143:62381143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1928delA
AA Mutation	p.Lys643ArgfsTer4(p.K643Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000401507
Start	62357708:62357709(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.682_683dupGT
AA Mutation	p.Arg229Ter(p.R229*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62357728:62357728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>A
AA Mutation	p.Arg231Gln(p.R231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401507
Start	62348140:62348140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000401507
Start	62363241:62363241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183C>T
AA Mutation	p.Gln395Ter(p.Q395*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript