Colon Cancer: Gene >> ZIK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590062:57590062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251C>A
AA Mutation	p.Ser84Tyr(p.S84Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590425:57590425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556272973
CDS Mutation	c.614G>A
AA Mutation	p.Arg205His(p.R205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590460:57590460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>A
AA Mutation	p.Gly217Arg(p.G217R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590314:57590314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568671837
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590668:57590668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761232368
CDS Mutation	c.857G>A
AA Mutation	p.Arg286Gln(p.R286Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590353:57590353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368879763
CDS Mutation	c.542G>A
AA Mutation	p.Arg181Gln(p.R181Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57588558:57588558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92A>G
AA Mutation	p.Asp31Gly(p.D31G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590556:57590556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762570199
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Cys(p.R249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590049:57590049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238G>A
AA Mutation	p.Asp80Asn(p.D80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57591146:57591146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1335C>G
AA Mutation	p.Ser445Arg(p.S445R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000597850
Start	57588601:57588601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000597850
Start	57590584:57590585(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.777_778delAG
AA Mutation	p.Arg259SerfsTer12(p.R259Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000597850
Start	57591132:57591132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321G>T
AA Mutation	p.Gly441Ter(p.G441*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000597850
Start	57588602:57588602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>T
AA Mutation	p.Glu46Ter(p.E46*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000597850
Start	57584390:57584390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZIK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590313:57590313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199973825
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590907:57590907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>A
AA Mutation	p.Leu366Ile(p.L366I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590387:57590387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576G>T
AA Mutation	p.Lys192Asn(p.K192N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000597850
Start	57590667:57590667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768606203
CDS Mutation	c.856C>T
AA Mutation	p.Arg286Trp(p.R286W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript