Colon Cancer: Gene >> INCENP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62145233:62145233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780G>A
AA Mutation	p.Glu594Lys(p.E594K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62145652:62145652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860G>T
AA Mutation	p.Glu620Asp(p.E620D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62129998:62129998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471G>T
AA Mutation	p.Glu157Asp(p.E157D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62148540:62148540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2269G>A
AA Mutation	p.Glu757Lys(p.E757K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62128172:62128172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779937744
CDS Mutation	c.11C>T
AA Mutation	p.Thr4Met(p.T4M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62130387:62130387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535973051
CDS Mutation	c.860C>T
AA Mutation	p.Pro287Leu(p.P287L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62148812:62148812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2357C>T
AA Mutation	p.Ala786Val(p.A786V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62130416:62130416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768284528
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Cys(p.R297C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62151768:62151768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781470064
CDS Mutation	c.2549C>T
AA Mutation	p.Pro850Leu(p.P850L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62129892:62129892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151321132
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62145016:62145016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771853715
CDS Mutation	c.1640G>A
AA Mutation	p.Arg547Gln(p.R547Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394818
Start	62138932:62138932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394818
Start	62128272:62128272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394818
Start	62129878:62129878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394818
Start	62140274:62140274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138752017
CDS Mutation	c.1332G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394818
Start	62148780:62148780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2325G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> INCENP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394818
Start	62130071:62130071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544C>G
AA Mutation	p.His182Asp(p.H182D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript