Colon Cancer: Gene >> ELK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96247693:96247693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Ile(p.L321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96247666:96247666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>A
AA Mutation	p.Gly312Ser(p.G312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96223580:96223580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14T>C
AA Mutation	p.Ile5Thr(p.I5T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96259809:96259809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1081C>T
AA Mutation	p.Pro361Ser(p.P361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96247178:96247178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446A>T
AA Mutation	p.Asn149Ile(p.N149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96223571:96223571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5A>T
AA Mutation	p.Glu2Val(p.E2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96247220:96247220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1064000
CDS Mutation	c.488C>T
AA Mutation	p.Thr163Met(p.T163M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96223635:96223635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.69G>C
AA Mutation	p.Leu23Phe(p.L23F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96223709:96223709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96259756:96259756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758120639
CDS Mutation	c.1028C>T
AA Mutation	p.Pro343Leu(p.P343L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228741
Start	96247380:96247380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200581571
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228741
Start	96247344:96247344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201595118
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228741
Start	96247606:96247606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.879delA
AA Mutation	p.Lys293AsnfsTer49(p.K293Nfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228741
Start	96247251:96247251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.525delC
AA Mutation	p.Val176TrpfsTer7(p.V176Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ELK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228741
Start	96246995:96246995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263C>T
AA Mutation	p.Pro88Leu(p.P88L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript