Colon Cancer: Gene >> ILKAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254654
Start	238188221:238188221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335C>G
AA Mutation	p.Ala112Gly(p.A112G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254654
Start	238170613:238170613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102A>C
AA Mutation	p.Asn368His(p.N368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254654
Start	238170946:238170946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372551657
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ILKAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254654
Start	238184077:238184077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>C
AA Mutation	p.Cys190Ser(p.C190S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254654
Start	238170668:238170668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141848989
CDS Mutation	c.1047G>T
AA Mutation	p.Lys349Asn(p.K349N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254654
Start	238185282:238185282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431G>A
AA Mutation	p.Arg144Gln(p.R144Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254654
Start	238188159:238188159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758284655
CDS Mutation	c.397G>A
AA Mutation	p.Glu133Lys(p.E133K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254654
Start	238182070:238182070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773406326
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript